U.S. patent number 10,053,471 [Application Number 15/543,242] was granted by the patent office on 2018-08-21 for azabenzimidazole derivatives.
This patent grant is currently assigned to Boehringer Ingelheim International GmbH. The grantee listed for this patent is Boehringer Ingelheim International GmbH. Invention is credited to Frank Himmelsbach, Elke Langkopf.
United States Patent |
10,053,471 |
Himmelsbach , et
al. |
August 21, 2018 |
Azabenzimidazole derivatives
Abstract
The present invention relates to compounds of general formula
(I), wherein R.sup.1, R.sup.2, R.sup.3, A.sup.1, A.sup.2, m and n
are defined as in claim 1, which have valuable pharmacological
properties, in particular bind to the AMP-activated protein kinase
(AMPK) and modulate its activity. The compounds are suitable for
treatment and prevention of diseases which can be influenced by
this receptor, such as metabolic diseases, in particular diabetes
type 2. ##STR00001##
Inventors: |
Himmelsbach; Frank
(Mittelbiberach, DE), Langkopf; Elke (Biberach an der
Riss, DE) |
Applicant: |
Name |
City |
State |
Country |
Type |
Boehringer Ingelheim International GmbH |
Ingelheim am Rhein |
N/A |
DE |
|
|
Assignee: |
Boehringer Ingelheim International
GmbH (Ingelheim am Rhein, DE)
|
Family
ID: |
55129871 |
Appl.
No.: |
15/543,242 |
Filed: |
January 13, 2016 |
PCT
Filed: |
January 13, 2016 |
PCT No.: |
PCT/EP2016/050557 |
371(c)(1),(2),(4) Date: |
July 13, 2017 |
PCT
Pub. No.: |
WO2016/113299 |
PCT
Pub. Date: |
July 21, 2016 |
Prior Publication Data
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|
|
|
Document
Identifier |
Publication Date |
|
US 20180002349 A1 |
Jan 4, 2018 |
|
Foreign Application Priority Data
|
|
|
|
|
Jan 16, 2015 [EP] |
|
|
15151419 |
May 11, 2015 [EP] |
|
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15167116 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61P
3/10 (20180101); A61K 45/06 (20130101); C07D
519/00 (20130101); A61P 43/00 (20180101); A61K
31/437 (20130101); A61P 3/06 (20180101); A61P
3/04 (20180101); A61P 9/00 (20180101) |
Current International
Class: |
C07D
401/14 (20060101); A61K 31/437 (20060101); A61K
45/06 (20060101); C07D 519/00 (20060101) |
Field of
Search: |
;546/119 ;514/303 |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
Other References
Written Opinion of International Searching Authority for
PCT/EP2016050557, Form PCT/ISA 237, dated Aug. 3, 2016. cited by
applicant .
International Search report, for PCT/EP2016/050558, Form
PCT/ISA220, dated Aug. 3, 2016. cited by applicant .
Abstract for WO2014069426, May 8, 2014. cited by applicant.
|
Primary Examiner: Rahmani; Niloofar
Attorney, Agent or Firm: Wittmayer; Paula K. Kershner; David
L.
Claims
The invention claimed is:
1. A compound of formula I containing three (consecutive) aromatic
or heteroaromatic moieties ##STR00055## wherein A.sup.1 is selected
from the group consisting of CH, CR.sup.2 and N, A.sup.2 is
selected from the group consisting of CH, CF and N, R.sup.1 is
selected from the group consisting of F and Cl, R.sup.2 is selected
from the group consisting of F and methoxy, R.sup.3 is selected
from the group consisting of ##STR00056## m is selected from an
integer consisting of 0, 1 and 2, and n is selected from an integer
consisting of 0, 1, and 2, with the provisos, that at least one
substituent attached to an aromatic or heteroaromatic moiety in
formula I represents F or that R.sup.2 represents methoxy, or a
salt thereof.
2. A compound according to claim 1 with the substructure of formula
II containing a biphenylyl-azabenzimidazole moiety ##STR00057##
wherein R.sup.1 is selected from the group consisting of F and Cl,
m is selected from an integer consisting of 0, 1 and 2, and n is
selected from an integer consisting of 0, 1, and 2, with the
proviso, that at least one substituent attached to the
biphenylyl-azabenzimidazole moiety represents F, or a salt
thereof.
3. A compound according to claim 1 with the substructure of formula
III containing a biphenylyl-azabenzimidazole moiety ##STR00058##
wherein R.sup.1 is selected from the group consisting of F and Cl,
m is selected from an integer consisting of 0, 1 and 2, and n is
selected from an integer consisting of 0, 1, and 2, with the
proviso, that at least one substituent attached to the
biphenylyl-azabenzimidazole moiety represents F, or a salt
thereof.
4. A compound according to claim 1 with the substructure of formula
IV ##STR00059## wherein R.sup.1 is selected from the group
consisting of F and Cl, and n is selected from an integer
consisting of 0, 1, and 2, or a salt thereof.
5. A compound according to claim 1 with the substructure of formula
V ##STR00060## wherein R.sup.3 is selected from the group
consisting of ##STR00061## m is selected from an integer consisting
of 0, 1 and 2, and n is selected from an integer consisting of 0,
1, and 2, or a salt thereof.
6. A compound according to claim 1 with the substructure of formula
VI ##STR00062## wherein R.sup.3 is selected from the group
R.sup.3-G1 consisting of ##STR00063## m is selected from an integer
consisting of 0, 1 and 2, and n is selected from an integer
consisting of 0, 1, and 2, with the proviso, that at least one of m
and n denotes 1 or 2, or a salt thereof.
7. A pharmaceutically acceptable salt of a compound according to
claim 1.
8. A pharmaceutical composition comprising one or more compounds
according to claim 1 or one or more pharmaceutically acceptable
salts thereof, optionally together with one or more inert carriers
and/or diluents.
9. A method for treating diseases or conditions which can be
influenced by the modulation of the function of AMP-activated
protein kinase (AMPK), comprising administering a compound
according to claim 1 or a pharmaceutically acceptable salt thereof
to a patient in need thereof, wherein the disease or condition is
type 2 diabetes mellitus, insulin resistance, obesity,
cardiovascular disease, or dyslipidemia.
10. A pharmaceutical composition comprising one or more compounds
according to claim 1 or one or more pharmaceutically acceptable
salts thereof and one or more additional therapeutic agents,
optionally together with one or more inert carriers and/or
diluents.
11. The pharmaceutical composition according to claim 10, wherein
the one or more additional therapeutic agents is selected from the
group consisting of antidiabetic agents, agents for the treatment
of overweight and/or obesity and agents for the treatment of high
blood pressure, heart failure and/or atherosclerosis.
Description
FIELD OF THE INVENTION
The present invention relates to novel azabenzimidazole derivatives
that are agonists of the AMP-activated protein kinase (AMPK), to
processes for their preparation, to pharmaceutical compositions
containing these compounds and to their medical use for the
prophylaxis and/or treatment of diseases which can be influenced by
the modulation of the function of AMPK. Particularly, the
pharmaceutical compositions of the invention are suitable for the
prophylaxis and/or therapy of metabolic diseases, such as diabetes,
more specifically type 2 diabetes mellitus, and conditions
associated with the disease, including insulin resistance, obesity,
cardiovascular disease, dyslipidemia and kidney diseases such as
diabetic nephropathy and chronic kidney disease.
BACKGROUND OF THE INVENTION
Metabolic diseases are diseases caused by an abnormal metabolic
process and may either be congenital due to an inherited enzyme
abnormality or acquired due to a disease of an endocrine organ or
failure of a metabolically important organ such as the liver or the
pancreas.
Diabetes mellitus is a disease state or process derived from
multiple causative factors and is defined as a chronic
hyperglycemia associated with resulting damages to organs and
dysfunctions of metabolic processes. Depending on its etiology, one
differentiates between several forms of diabetes, which are either
due to an absolute (lacking or decreased insulin secretion) or to a
relative lack of insulin. Diabetes mellitus Type I (IDDM,
insulin-dependent diabetes mellitus) generally occurs in
adolescents under 20 years of age. It is assumed to be of
auto-immune etiology, leading to an insulitis with the subsequent
destruction of the beta cells of the islets of Langerhans which are
responsible for the insulin synthesis. In addition, in latent
autoimmune diabetes in adults (LADA; Diabetes Care. 8: 1460-1467,
2001) beta cells are being destroyed due to autoimmune attack. The
amount of insulin produced by the remaining pancreatic islet cells
is too low, resulting in elevated blood glucose levels
(hyperglycemia). Diabetes mellitus Type II generally occurs at an
older age. It is above all associated with a resistance to insulin
in the liver and the skeletal muscles, but also with a defect of
the islets of Langerhans. High blood glucose levels (and also high
blood lipid levels) in turn lead to an impairment of beta cell
function and to an increase in beta cell apoptosis.
Persistent or inadequately controlled hyperglycemia is associated
with a wide range of pathologies. Diabetes is a very disabling
disease, because today's common antidiabetic drugs do not control
blood sugar levels well enough to completely prevent the occurrence
of high and low blood sugar levels. Out of range blood sugar levels
are toxic and cause long-term complications for example
retinopathy, nephropathy, neuropathy and peripheral vascular
disease. There is also a host of related conditions, such as
obesity, hypertension, stroke, heart disease and hyperlipidemia,
for which persons with diabetes are substantially at risk.
Obesity is associated with an increased risk of follow-up diseases
such as cardiovascular diseases, hypertension, diabetes,
hyperlipidemia and an increased mortality. Diabetes (insulin
resistance) and obesity are part of the "metabolic syndrome" which
is defined as the linkage between several diseases (also referred
to as syndrome X, insulin-resistance syndrome, or deadly quartet).
These often occur in the same patients and are major risk factors
for development of diabetes type II and cardiovascular disease. It
has been suggested that the control of lipid levels and glucose
levels is required to treat diabetes type II, heart disease, and
other occurrences of metabolic syndrome (see e.g., Diabetes 48:
1836-1841, 1999; JAMA 288: 2209-2716, 2002).
Sensing and regulating cellular the energy status in response to
environmental and/or nutritional stress is highly important and
AMP-activated protein kinase (AMPK) is a major contributor for this
task (Hardie et al. (2001) Bioessays 23: 1112; Kemp et al. (2003)
Biochem. Soc. Transactions 31: 162). Cellular energy depletion
leads to the activation of AMP-activated protein kinase (AMPK)
thereby inhibiting ATP consuming and upregulating ATP generating
pathways. On a cellular level several substrates are regulated by
AMP-activated protein kinase (AMPK) such as acetyl-CoA-carboxylase
(ACC) and HMG-CoA-reductase (Carling et al. (1987) FEBS Letters
223: 217), hormone-sensitive lipase (Garton et al. (1989) Eur. J.
Biochem. 179: 249), malonyl-CoA-decarboxylase (Saha et al. (2000)
J. Biol. Chem. 275: 24279) and glycerol-3-phosphate acyltransferase
(Muoio et al. (1999) Biochem. J. 338: 783).
AMP-activated protein kinase (AMPK) mediated phosphorylation of ACC
leads to inhibition of ACC, which then results in a decrease of
fatty acid synthesis while fatty acid oxidation is increased.
AMP-activated protein kinase (AMPK) mediated phosphorylation and
inhibition of HMG-CoA-reductase leads to a decrease in cholesterol
synthesis. Triacylglycerol synthesis and fatty acid oxidation is
regulated by AMP-activated protein kinase (AMPK) via
glycerol-3-phosphate acyltransferase. In addition AMP-activated
protein kinase (AMPK) stimulates glucose transport in skeletal
muscle and regulates the expression of genes involved in fatty acid
and glucose metabolism (Hardie et al. (2001) Bioessays 23: 1112;
Kemp et al. (2003) Biochem. Soc. Transactions 31: 162). Glucose
homeostasis is mediated in liver and muscle by AMP-activated
protein kinase (AMPK), wherein activation of AMP-activated protein
kinase (AMPK) leads to an increase in GLUT 4-dependent glucose
uptake (Sakamoto et al. (2008) Am. J. Physiol. Endocrinol. Metab.
295: E29-E37; Karagounis et al. (2009) Int. J. Biochem. Cell Biol.
41: 2360-2363; Pehmoller et al. (2009) Am. J. Physiol. Endocrinol.
Metab. 297: E665-E675).
Besides energy regulation on a cellular level AMP-activated protein
kinase (AMPK) also regulates whole body energy metabolism.
Independently of the cellular AMP level AMP-activated protein
kinase (AMPK) can be activated by the adipocyte derived hormones
leptin (Minokoski et al. (2002) Nature 415: 339) and adiponectin
(Yamauchi et al. (2002) Nature Medicine 8: 1288).
From the points discussed above activation of AMP-activated protein
kinase (AMPK) in vivo is expected to result in hepatic stimulation
of fatty acid oxidation; inhibition of cholesterol synthesis,
lipogenesis and triglyceride synthesis; stimulation of skeletal
muscle fatty acid oxidation and glucose uptake; improved insulin
action; increase in energy expenditure and hence a decrease in body
weight.
OBJECT OF THE PRESENT INVENTION
The object of the present invention is to provide new compounds,
hereinafter described as compounds of formula I, in particular new
azabenzimidazole derivatives, which are active with regard to the
AMP-activated protein kinase (AMPK), notably are agonists of the
AMP-activated protein kinase (AMPK).
A further object of the present invention is to provide new
compounds, in particular new azabenzimidazole derivatives, which
have an activating effect on the AMP-activated protein kinase
(AMPK) in vitro and/or in vivo and possess suitable pharmacological
and pharmacokinetic properties to use them as medicaments.
A further object of the present invention is to provide effective
agonists of AMP-activated protein kinase (AMPK), in particular for
the treatment of metabolic disorders, for example diabetes,
dyslipidemia and/or obesity.
A further object of the present invention is to provide methods for
treating a disease or condition mediated by the activation the
AMP-activated protein kinase (AMPK) in a patient.
A further object of the present invention is to provide a
pharmaceutical composition comprising at least one compound
according to the invention.
A further object of the present invention is to provide a
combination of at least one compound according to the invention
with one or more additional therapeutic agents.
Further objects of the present invention become apparent to the one
skilled in the art by the description hereinbefore and in the
following and by the examples.
AMP-activated protein kinase (AMPK) modulators are known in the
art, for example, the compounds disclosed in WO 2012033149, WO
2012116145, WO 2013153479, WO 2014031515 and WO 2014069426. The
azabenzimidazole derivatives of the present invention may provide
several advantages, such as enhanced potency and/or efficacy, high
metabolic and/or chemical stability, favorable pharmacokinetic
profile, high selectivity and/or tolerability and in consequence
low toxicity, reduced risk to cause adverse events or undesirable
side effects, and enhanced solubility.
SUMMARY OF THE INVENTION
In a first aspect the invention relates to compounds of formula I
containing three (consecutive) aromatic or heteroaromatic
moieties
##STR00002## wherein R.sup.1 is selected from the group R.sup.1-G1
consisting of F and Cl, R.sup.2 is selected from the group
R.sup.2-G1 consisting of F and methoxy, R.sup.3 is selected from
the group R.sup.3-G1 consisting of
##STR00003## A.sup.1 is selected from the group A.sup.1-G1
consisting of CH, CR.sup.2 and N, A.sup.2 is selected from the
group A.sup.2-G1 consisting of CH, CF and N, m is selected from an
integer consisting of 0, 1 and 2, and n is selected from an integer
consisting of 0, 1, and 2, with the provisos, that at least one
substituent attached to an aromatic or heteroaromatic moiety in
formula I represents F or that R.sup.2 represents methoxy, the
isoforms, tautomers, stereoisomers, metabolites, prodrugs,
solvates, hydrates, and the salts thereof, particularly the
physiologically acceptable salts thereof with inorganic or organic
acids or bases, or the combinations thereof.
The extension -Gn used within the definitions is meant to identify
genus n of the respective substituent. For example, R.sup.1-G1
defines genus 1 of the substituent R.sup.1.
In a further aspect this invention relates to a pharmaceutical
composition, comprising one or more compounds of general formula I
or one or more pharmaceutically acceptable salts thereof according
to the invention, optionally together with one or more inert
carriers and/or diluents.
In a further aspect this invention relates to a method for treating
diseases or conditions which are mediated by activating the
AMP-activated protein kinase (AMPK) in a patient in need thereof
characterized in that a compound of general formula I or a
pharmaceutically acceptable salt thereof is administered to the
patient.
According to another aspect of the invention, there is provided a
method for treating a metabolic disease or disorder, such as
diabetes, dyslipidemia and/or obesity, in a patient in need thereof
characterized in that a therapeutically effective amount of a
compound of general formula I or a pharmaceutically acceptable salt
thereof is administered to the patient.
According to another aspect of the invention, there is provided a
method for treating a cardiovascular disease or disorder, such as
myocardial infarction, stroke, heart failure, coronary artery
disease, hypertension, in a patient in need thereof characterized
in that a therapeutically effective amount of a compound of general
formula I or a pharmaceutically acceptable salt thereof is
administered to the patient.
According to another aspect of the invention, there is provided a
method for treating a kidney disease or disorder, such as diabetic
nephropathy, chronic kidney disease, acute kidney injury and/or
polycystic kidney disease, in a patient in need thereof
characterized in that a therapeutically effective amount of a
compound of general formula I or a pharmaceutically acceptable salt
thereof is administered to the patient.
According to another aspect of the invention, there is provided the
use of a compound of the general formula I or a pharmaceutically
acceptable salt thereof for the manufacture of a medicament for a
therapeutic method as described hereinbefore and hereinafter.
According to another aspect of the invention, there is provided a
compound of the general formula I or a pharmaceutically acceptable
salt thereof for use in a therapeutic method as described
hereinbefore and hereinafter.
In a further aspect this invention relates to a method for treating
a disease or condition mediated by the activation of the
AMP-activated protein kinase (AMPK) in a patient that includes the
step of administering to the patient in need of such treatment a
therapeutically effective amount of a compound of the general
formula I or a pharmaceutically acceptable salt thereof in
combination with a therapeutically effective amount of one or more
additional therapeutic agents.
In a further aspect this invention relates to the use of a compound
of the general formula I or a pharmaceutically acceptable salt
thereof in combination with one or more additional therapeutic
agents for the treatment of diseases or conditions which are
mediated by the activation of the AMP-activated protein kinase
(AMPK).
In a further aspect this invention relates to a pharmaceutical
composition which comprises a compound according to general formula
I or a pharmaceutically acceptable salt thereof and one or more
additional therapeutic agents, optionally together with one or more
inert carriers and/or diluents.
Other aspects of the invention become apparent to the one skilled
in the art from the specification and the experimental part as
described hereinbefore and hereinafter.
DETAILED DESCRIPTION
Unless otherwise stated, the groups, residues, and substituents,
particularly R.sup.1, R.sup.2, R.sup.3, A.sup.1 and A.sup.2 are
defined as above and hereinafter. If residues, substituents, or
groups occur several times in a compound, they may have the same or
different meanings. Some preferred meanings of individual groups
and substituents of the compounds according to the invention will
be given hereinafter. Any and each of these definitions may be
combined with each other.
R.sup.1:
R.sup.1-G1:
The group R.sup.1 is preferably selected from the group R.sup.1-G1
as defined hereinbefore.
R.sup.1-G2a:
In another embodiment the group R.sup.1 is selected from the group
R.sup.1-G2a consisting of F.
R.sup.1-G2b:
In another embodiment the group R.sup.1 is selected from the group
R.sup.1-G2b consisting of Cl.
R.sup.2:
R.sup.2-G1:
The group R.sup.2 is preferably selected from the group R.sup.2-G1
as defined hereinbefore.
R.sup.2-G2a:
In another embodiment the group R.sup.2 is selected from the group
R.sup.2-G2a consisting of F.
R.sup.2-G2b:
In another embodiment the group R.sup.2 is selected from the group
R.sup.2-G2b consisting of methoxy.
R.sup.3:
R.sup.3-G1:
The group R.sup.3 is preferably selected from the group R.sup.3-G1
as defined hereinbefore.
R.sup.3-G2a:
In another embodiment the group R.sup.3 is selected from the group
R.sup.3-G2a consisting of
##STR00004## R.sup.3-G2b:
In another embodiment the group R.sup.3 is selected from the group
R.sup.3-G2b consisting of
##STR00005## A.sup.1: A.sup.1-G1:
The group A.sup.1 is preferably selected from the group A.sup.1-G1
as defined hereinbefore.
A.sup.1-G2a:
In another embodiment the group A.sup.1 is selected from the group
A.sup.1-G2a consisting of CH and CR.sup.2.
A.sup.1-G2b:
In another embodiment the group A.sup.1 is selected from the group
A.sup.1-G2b consisting of N.
A.sup.2:
A.sup.2-G1:
The group A.sup.1 is preferably selected from the group A.sup.2-G1
as defined hereinbefore.
A.sup.2-G2a:
In another embodiment the group A.sup.2 is selected from the group
A.sup.2-G2a consisting of CH and CF.
A.sup.2-G2b:
In another embodiment the group A.sup.2 is selected from the group
A.sup.2-G2b consisting of N.
PREFERRED EMBODIMENTS
In a preferred embodiment the invention relates to compounds of
formula II containing a biphenylyl-azabenzimidazole moiety
##STR00006## wherein R.sup.1 is selected from the group R.sup.1-G1
consisting of F and Cl, m is selected from an integer consisting of
0, 1 and 2, and n is selected from an integer consisting of 0, 1,
and 2, with the proviso, that at least one substituent attached to
the biphenylyl-azabenzimidazole moiety represents F, the isoforms,
tautomers, stereoisomers, metabolites, prodrugs, solvates,
hydrates, and the salts thereof, particularly the physiologically
acceptable salts thereof with inorganic or organic acids or bases,
or the combinations thereof.
In another preferred embodiment the invention relates to compounds
of formula III containing a biphenylyl-azabenzimidazole moiety
##STR00007## wherein R.sup.1 is selected from the group R.sup.1-G1
consisting of F and Cl, m is selected from an integer consisting of
0, 1 and 2, and n is selected from an integer consisting of 0, 1,
and 2, with the proviso, that at least one substituent attached to
the biphenylyl-azabenzimidazole moiety represents F, the isoforms,
tautomers, stereoisomers, metabolites, prodrugs, solvates,
hydrates, and the salts thereof, particularly the physiologically
acceptable salts thereof with inorganic or organic acids or bases,
or the combinations thereof.
In another preferred embodiment the invention relates to compounds
of formula IV
##STR00008## wherein R.sup.1 is selected from the group R.sup.1-G1
consisting of F and Cl, and n is selected from an integer
consisting of 0, 1, and 2, the isoforms, tautomers, stereoisomers,
metabolites, prodrugs, solvates, hydrates, and the salts thereof,
particularly the physiologically acceptable salts thereof with
inorganic or organic acids or bases, or the combinations
thereof.
In another preferred embodiment the invention relates to compounds
of formula V
##STR00009## wherein R.sup.3 is selected from the group R.sup.3-G1
consisting of
##STR00010## m is selected from an integer consisting of 0, 1 and
2, and n is selected from an integer consisting of 0, 1, and 2, the
isoforms, tautomers, stereoisomers, metabolites, prodrugs,
solvates, hydrates, and the salts thereof, particularly the
physiologically acceptable salts thereof with inorganic or organic
acids or bases, or the combinations thereof.
In another preferred embodiment the invention relates to compounds
of formula VI
##STR00011## wherein R.sup.3 is selected from the group R.sup.3-G1
consisting of
##STR00012## m is selected from an integer consisting of 0, 1 and
2, and n is selected from an integer consisting of 0, 1, and 2,
with the proviso, that at least one of m and n denotes 1 or 2, the
isoforms, tautomers, stereoisomers, metabolites, prodrugs,
solvates, hydrates, and the salts thereof, particularly the
physiologically acceptable salts thereof with inorganic or organic
acids or bases, or the combinations thereof.
Particularly preferred compounds, including their tautomers and
stereoisomers, the salts thereof, or any solvates or hydrates
thereof, are described in the experimental section hereinafter.
The compounds according to the invention and their intermediates
may be obtained using methods of synthesis which are known to the
one skilled in the art and described in the literature of organic
synthesis. Preferably the compounds are obtained analogously to the
methods of preparation explained more fully hereinafter, in
particular as described in the experimental section. In some cases
the sequence adopted in carrying out the reaction schemes may be
varied. Variants of these reactions that are known to the skilled
man but are not described in detail here may also be used. The
general processes for preparing the compounds according to the
invention will become apparent to the skilled person on studying
the schemes that follow. Starting compounds are commercially
available or may be prepared by methods that are described in the
literature or herein, or may be prepared in an analogous or similar
manner. Before the reaction is carried out any corresponding
functional groups in the compounds may be protected using
conventional protecting groups. These protecting groups may be
cleaved again at a suitable stage within the reaction sequence
using methods familiar to the skilled person.
The compounds of the invention I are preferably accessed from a
precursor 1a or 1b which bears a protecting group at the
imidazopyridine-nitrogen in position 3 or 1 (Scheme 1); A.sup.1,
A.sup.2, R.sup.1, R.sup.2, R.sup.3 and R.sup.3' have the meaning as
defined hereinbefore and hereinafter. For the sake of convenience
only the N.sup.3 protected species (1a in Scheme 1) will be shown
hereinafter, although by and large all transformations described
below are also applicable to the N.sup.1 protected series (1b in
Scheme 1).
##STR00013##
The benzyl protecting group is cleaved advantageously using
hydrogen in the presence of a transition metal, preferably
palladium on carbon in a solvent such as methanol, ethanol,
tetrahydrofuran, 1,4-dioxane. Benzyl groups bearing electron
donating groups on the phenyl ring, such as methoxy, may also be
removed under acidic conditions such as H.sub.2SO.sub.4 or
CF.sub.3CO.sub.2H, MeSO.sub.3H. Amino-acetal derivatives can be
cleaved under acidic conditions such as HCl, H.sub.2SO.sub.4,
CF.sub.3CO.sub.2H, MeSO.sub.3H, KHSO.sub.4, HCO.sub.2H,
BF.sub.3.times.OEt.sub.2 in a solvent such as dichloromethane,
water, tetrahydrofuran, 1,4-dioxane or mixtures thereof at -10 to
100.degree. C. In addition to cleavage under acidic conditions,
amino-acetal derivatives bearing a Si(CH.sub.3).sub.3 group can
also be cleaved in the presence of tetrabutylammonium fluoride.
The N atom of the sulfoximine moiety R.sup.3 might be protected
with a suitable protecting group PG.sup.2, e.g. a
benzyloxy-carbonyl, tert-butoxycarbonyl, acetyl, or
2,2,2-trifluoroacetyl group. The protecting group PG.sup.2 is
either removed together with PG.sup.1 in one reaction step or in an
additional deprotection step, depending on the nature of PG.sup.1
and PG.sup.2. The benzyloxy-carbonyl group is cleaved
advantageously using hydrogen in the presence of a transition
metal, preferably palladium on carbon in a solvent such as
methanol, ethanol, tetrahydrofuran, 1,4-dioxane. The
tert.-butyloxycarbonyl group can be cleaved under acidic conditions
such as HCl, H.sub.2SO.sub.4, CF.sub.3CO.sub.2H, MeSO.sub.3H,
KHSO.sub.4, HCO.sub.2H, BF.sub.3.times.OEt.sub.2 in a solvent such
as dichloromethane, water, tetrahydrofuran, 1,4-dioxane or mixtures
thereof at -10 to 100.degree. C. The 2,2,2-trifluoroacetyl group
can be cleaved under basic conditions such as K.sub.2CO.sub.3,
NaOH, KOH, NaOMe, NaOEt, NaOtBu in a solvent such as water,
methanol, tetrahydrofuran, 1,4-dioxane or mixtures thereof at -10
to 50.degree. C.
Compounds 1 can be prepared from imidazopyridine derivatives 2 and
boronic acid derivatives 3 (Scheme 2); A.sup.1, A.sup.2, R.sup.1,
R.sup.2, R.sup.3' have the meaning defined hereinbefore and
hereinafter.
##STR00014##
The reaction is preferably conducted with a palladium derived
catalyst, e.g.
[1,1'-bis(diphenylphosphino)-ferrocene]-dichloropalladium(II)-CH.sub-
.2Cl.sub.2-complex (PdCl.sub.2(dppf).times.CH.sub.2Cl.sub.2) in the
presence of a base, e.g. sodium carbonate, in a solvent like
tetrahydrofuran, 1,4-dioxane, toluene, water, N,N-dimethylformamide
or mixtures thereof, at 40 to 120.degree. C.
Alternatively, compounds 1 can be prepared in a stepwise approach
by successively linking the aryl or heteroaryl groups to the
imidazopyridine (Scheme 3) using essentially the same reaction
conditions as described for Scheme 2; A.sup.1, A.sup.2, R.sup.1,
R.sup.2, R.sup.3' have the meaning defined hereinbefore and
hereinafter.
##STR00015##
Compounds 1' bearing a sulfoximine linked via the nitrogen to an
aryl or heteroaryl group can be prepared from halogen compounds 10
via direct coupling of the sulfoximine (Scheme 4); A.sup.1,
A.sup.2, R.sup.1, R.sup.2 have the meaning defined hereinbefore and
hereinafter.
##STR00016##
The coupling reaction is preferably conducted with a palladium
derived catalyst and a suitable ligand, e.g.
tris(dibenzylideneacetone)dipalladium(0) and
4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (Xantphos) or
2-(di-t-butylphosphino)bipheny, palladium(II) acetate and
2-dicyclohexylphosphino-2',6'-di-isopropoxy-1,1'-biphenyl (RuPhos),
or palladium(II) acetate and racemic
2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl in the presence of a
base, e.g. cesium carbonate or sodium tert-butoxide in a suitable
solvent such as 1,4-dioxane or toluene at 40 to 120.degree. C.
The synthetic routes presented may rely on the use of protecting
groups. For example, potentially reactive groups present, such as
hydroxy, carbonyl, carboxy, amino, alkylamino, or imino, may be
protected during the reaction by conventional protecting groups
which are cleaved again after the reaction. Suitable protecting
groups for the respective functionalities and their removal are
well known to the one skilled in the art and are described in the
literature of organic synthesis.
The compounds of general formula I may be resolved into their
enantiomers and/or diastereomers as mentioned below. Thus, for
example, cis/trans mixtures may be resolved into their cis and
trans isomers and racemic compounds may be separated into their
enantiomers.
The cis/trans mixtures may be resolved, for example, by
chromatography into the cis and trans isomers thereof. The
compounds of general formula I which occur as racemates may be
separated by methods known per se into their optical antipodes and
diastereomeric mixtures of compounds of general formula I may be
resolved into their diastereomers by taking advantage of their
different physicochemical properties using methods known per se,
e.g. chromatography and/or fractional crystallization; if the
compounds obtained thereafter are racemates, they may be resolved
into the enantiomers as mentioned below.
The racemates are preferably resolved by column chromatography on
chiral phases or by crystallization from an optically active
solvent or by reacting with an optically active substance which
forms salts or derivatives such as esters or amides with the
racemic compound. Salts may be formed with enantiomerically pure
acids for basic compounds and with enantiomerically pure bases for
acidic compounds. Diastereomeric derivatives are formed with
enantiomerically pure auxiliary compounds, e.g. acids, their
activated derivatives, or alcohols. Separation of the
diastereomeric mixture of salts or derivatives thus obtained may be
achieved by taking advantage of their different physico-chemical
properties, e.g. differences in solubility; the free antipodes may
be released from the pure diastereomeric salts or derivatives by
the action of suitable agents. Optically active acids commonly used
for such a purpose as well as optically active alcohols applicable
as auxiliary residues are known to those skilled in the art.
As mentioned above, the compounds of formula I may be converted
into salts, particularly for pharmaceutical use into the
pharmaceutically acceptable salts. As used herein,
"pharmaceutically acceptable salts" refer to derivatives of the
disclosed compounds wherein the parent compound is modified by
making acid or base salts thereof.
The compounds according to the invention are advantageously also
obtainable using the methods described in the examples that follow,
which may also be combined for this purpose with methods known to
the skilled man from the literature.
Terms and Definitions
Terms not specifically defined herein should be given the meanings
that would be given to them by one of skill in the art in light of
the disclosure and the context. As used in the specification,
however, unless specified to the contrary, the following terms have
the meaning indicated and the following conventions are adhered
to.
The terms "compound(s) according to this invention", "compound(s)
of formula (I)", "compound(s) of the invention" and the like denote
the compounds of the formula (I) according to the present invention
including their tautomers, stereoisomers and mixtures thereof and
the salts thereof, in particular the pharmaceutically acceptable
salts thereof, and the solvates and hydrates of such compounds,
including the solvates and hydrates of such tautomers,
stereoisomers and salts thereof.
The terms "treatment" and "treating" embrace both preventative,
i.e. prophylactic, or therapeutic, i.e. curative and/or palliative,
treatment. Thus the terms "treatment" and "treating" comprise
therapeutic treatment of patients having already developed said
condition, in particular in manifest form. Therapeutic treatment
may be symptomatic treatment in order to relieve the symptoms of
the specific indication or causal treatment in order to reverse or
partially reverse the conditions of the indication or to stop or
slow down progression of the disease. Thus the compositions and
methods of the present invention may be used for instance as
therapeutic treatment over a period of time as well as for chronic
therapy. In addition the terms "treatment" and "treating" comprise
prophylactic treatment, i.e. a treatment of patients at risk to
develop a condition mentioned hereinbefore, thus reducing said
risk.
When this invention refers to patients requiring treatment, it
relates primarily to treatment in mammals, in particular
humans.
The term "therapeutically effective amount" means an amount of a
compound of the present invention that (i) treats or prevents the
particular disease or condition, (ii) attenuates, ameliorates, or
eliminates one or more symptoms of the particular disease or
condition, or (iii) prevents or delays the onset of one or more
symptoms of the particular disease or condition described
herein.
The terms "modulated" or "modulating", or "modulate(s)", as used
herein, unless otherwise indicated, refer to the activation of the
AMP-activated protein kinase (AMPK) with one or more compounds of
the present invention.
The terms "mediated" or "mediating" or "mediate", as used herein,
unless otherwise indicated, refer to the (i) treatment, including
prevention of the particular disease or condition, (ii)
attenuation, amelioration, or elimination of one or more symptoms
of the particular disease or condition, or (iii) prevention or
delay of the onset of one or more symptoms of the particular
disease or condition described herein.
The term "substituted" as used herein, means that any one or more
hydrogens on the designated atom, radical or moiety is replaced
with a selection from the indicated group, provided that the atom's
normal valence is not exceeded, and that the substitution results
in an acceptably stable compound.
In case a compound of the present invention is depicted in form of
a chemical name and as a formula in case of any discrepancy the
formula shall prevail.
An asterisk may be used in sub-formulas to indicate the bond which
is connected to the core molecule as defined.
The numeration of the atoms of a substituent starts with the atom
which is closest to the core or to the group to which the
substituent is attached.
For example, the term "3-carboxypropyl-group" represents the
following substituent:
##STR00017## wherein the carboxy group is attached to the third
carbon atom of the propyl group. The terms "1-methylpropyl-",
"2,2-dimethylpropyl-" or "cyclopropylmethyl-" group represent the
following groups:
##STR00018##
The asterisk may be used in sub-formulas to indicate the bond which
is connected to the core molecule as defined.
Unless specifically indicated, throughout the specification and the
appended claims, a given chemical formula or name shall encompass
tautomers and all stereo, optical and geometrical isomers (e.g.
enantiomers, diastereomers, E/Z isomers etc.) and racemates thereof
as well as mixtures in different proportions of the separate
enantiomers, mixtures of diastereomers, or mixtures of any of the
foregoing forms where such isomers and enantiomers exist, as well
as salts, including pharmaceutically acceptable salts thereof and
solvates thereof such as for instance hydrates including solvates
of the free compounds or solvates of a salt of the compound.
The phrase "pharmaceutically acceptable" is employed herein to
refer to those compounds, materials, compositions, and/or dosage
forms which are, within the scope of sound medical judgment,
suitable for use in contact with the tissues of human beings and
animals without excessive toxicity, irritation, allergic response,
or other problem or complication, and commensurate with a
reasonable benefit/risk ratio.
As used herein, "pharmaceutically acceptable salts" refer to
derivatives of the disclosed compounds wherein the parent compound
is modified by making acid or base salts thereof.
Salts of other acids than those mentioned above which for example
are useful for purifying or isolating the compounds of the present
invention (e.g. trifluoro acetate salts) also comprise a part of
the invention.
Pharmacological Activity
The activity of the compounds of the invention may be demonstrated
using the following in vitro AMPK activation assays:
AMPK .alpha.1.beta.1.gamma.1:
Recombinant human AMPK (containing subunits alpha1, beta1 and
gamma1) was obtained from a baculovirus expression system. The 3
subunits were expressed together, affinity-purified via a GST-tag
fused to the alpha 1 subunit and deep-frozen in storage buffer (50
mM Tris-HCl pH 8, 300 mM NaCl, 1 mM TCEP and 10% glycerol) at
-80.degree. C. until use. The activity of the AMPK protein was
determined using the ADP Glo.RTM. Luminescence Kinase test
(Promega; V9103X). In this homogeneous test the amount of ADP
formed by the kinase reaction is quantified by a
luciferin-luciferase reaction using luminescence as read-out. The
luminescence signal obtained correlates with the amount of ADP
resulting from the kinase reaction and thus correlates with the
activity of the protein kinase.
Method:
The test compounds were dissolved in 100% DMSO at a concentration
of 10 mM and in a first step diluted in DMSO to a concentration of
5 mM, followed by serial dilution steps in 100% DMSO. Dilution
factor and number of dilution steps may vary. Typically 8 different
concentrations by 1:5 dilutions were prepared, further dilutions of
the substances were carried out with test buffer (20 mM Hepes (pH
7.0), 15 mM MgCl.sub.2, 0.025% BSA, 0.01% Brij 35) until a
concentration was reached which was 5 times above the final test
concentration. 2 .mu.l aliquots of these dilutions were transferred
into a 384-well Optiplate (Perkin Elmer, #6007290). Typically the
start concentration for serial dilutions in the assay is 10 .mu.M.
Typically AMPK was diluted to 25 .mu.g/ml in the test buffer and 4
.mu.l of this dilution were used in the kinase test (final
concentration of AMPK is 10 .mu.g/ml in a total volume of 10 .mu.l
for the kinase reaction). Kinase concentrations may vary depending
on activity of the preparation batches. After 10 minutes incubation
at room temperature 4 .mu.l of a mix containing 2.5 .mu.M substrate
(H-His-Met-Arg-Ser-Ala-Met-Ser-Gly-Leu-His-Leu-Val-Lys-Arg-Arg-OH
Trifluoroacetate salt/HMRSAMSGLHLVKRR from Bachem, Cat. No. H5938)
and 75 .mu.M ATP in test buffer were added to each well and the
incubation was continued for 60 minutes at room temperature.
Positive controls are the reaction mixtures that contain no test
substance; negative controls (blanks) are reaction mixtures that
contain no AMPK enzyme.
After 60 minutes, 10 .mu.l ADP-Glo.RTM. solution (ADP-Glo Reagent
#V912B Promega) (heated to room temperature) were added to each
well and incubation was continued for 40 minutes. Then 20 .mu.l
Kinase detection mix (Detection Buffer #V913B Promega; Kinase
Detection Substrate #V914B Promega) were added and incubated for
additional 40 minutes at room temperature.
All incubations were done in sealed plates in the dark.
The plates were read with an Envision Luminescence Reader
(Perkin-Elmer).
Data Evaluation and Calculation:
The output file of the reader is a csv file that contains the well
number and measured RLU. For data evaluation and calculation, the
measurement of the negative control was set as 0% control and the
measurement of the positive control was set as 100% control. Based
on these values the % value for the measurement of each substance
concentration was calculated using Assay Explorer software
(Accelrys). Activating compounds achieve % of control values above
100%. The IC.sub.50 values were calculated from the % control
values using Assay Explorer software. Calculation:
[y=(a-d)/(1+(x/c)^b)+d], a=low value, d=high value; x=conc M;
c=IC.sub.50 M; b=hill; y=% ctrl. The maximal achievable activation
of a compound in the tested concentration range is reported as
percent of control max (PoCmax).
The compounds according to the invention typically have EC.sub.50
values in the range from about 0.1 nM to about 10 .mu.M, preferably
less than 1 .mu.M, more preferably less than 300 nM.
EC.sub.50 and PoCmax values for compounds according to the
invention are shown in the following table. The number of the
compound corresponds to the number of the Example in the
experimental section.
TABLE-US-00001 AMPK .alpha.1.beta.1.gamma.1 AMPK
.alpha.1.beta.1.gamma.1 Example EC.sub.50 [nM] PoCmax [%] 1 284 540
2 115 496 3 302 480 4 3564 421 5 60 538 6 450 490 7 125 640 8 255
659 9 282 700 10 193 479 11 1200 423 12 109 608 13 71 523 14 68 484
15 344 426 16 74 475 17 84 475
In view of their ability to modulate the activity of the
AMP-activated protein kinase (AMPK), in particular an agonistic
activity, the compounds of general formula I according to the
invention, including the corresponding salts thereof, are
theoretically suitable for the treatment of all those diseases or
conditions which may be affected or which are mediated by the
activation of the AMP-activated protein kinase (AMPK).
Accordingly, the present invention relates to a compound of general
formula I as a medicament.
Furthermore, the present invention relates to the use of a compound
of general formula I or a pharmaceutical composition according to
this invention for the treatment and/or prevention of diseases or
conditions which are mediated by the activation of the
AMP-activated protein kinase (AMPK) in a patient, preferably in a
human.
In yet another aspect the present invention relates to a method for
treating a disease or condition mediated by the activation of the
AMP-activated protein kinase (AMPK) in a mammal that includes the
step of administering to a patient, preferably a human, in need of
such treatment a therapeutically effective amount of a compound or
a pharmaceutical composition of the present invention.
Diseases and conditions mediated by agonists of the AMP-activated
protein kinase (AMPK) embrace metabolic diseases or conditions.
According to one aspect the compounds and pharmaceutical
compositions of the present invention are particularly suitable for
treating diabetes mellitus, in particular Type 2 diabetes, Type
diabetes, complications of diabetes (such as e.g. retinopathy,
nephropathy or neuropathies, diabetic foot, ulcers or
macroangiopathies), metabolic acidosis or ketosis, reactive
hypoglycaemia, hyperinsulinaemia, glucose metabolic disorder,
insulin resistance, metabolic syndrome, dyslipidaemias of different
origins, atherosclerosis and related diseases, obesity, high blood
pressure, chronic heart failure, oedema and hyperuricaemia.
The compounds and pharmaceutical compositions of the present
invention are also suitable for preventing beta-cell degeneration
such as e.g. apoptosis or necrosis of pancreatic beta cells. The
compounds and pharmaceutical compositions of the present invention
are also suitable for improving or restoring the functionality of
pancreatic cells, and also for increasing the number and size of
pancreatic beta cells.
Therefore according to another aspect the invention relates to
compounds of formula I and pharmaceutical compositions according to
the invention for use in preventing, delaying, slowing the
progression of and/or treating metabolic diseases, particularly in
improving the glycaemic control and/or beta cell function in the
patient.
In another aspect the invention relates to compounds of formula I
and pharmaceutical compositions according to the invention for use
in preventing, delaying, slowing the progression of and/or treating
type 2 diabetes, overweight, obesity, complications of diabetes and
associated pathological conditions.
In addition the compounds and pharmaceutical compositions according
to the invention are suitable for use in one or more of the
following therapeutic processes: for preventing, delaying, slowing
the progression of or treating metabolic diseases, such as for
example type 1 diabetes, type 2 diabetes, insufficient glucose
tolerance, insulin resistance, hyperglycaemia, hyperlipidaemia,
hypercholesterolaemia, dyslipidaemia, syndrome X, metabolic
syndrome, obesity, high blood pressure, chronic systemic
inflammation, retinopathy, neuropathy, nephropathy,
atherosclerosis, endothelial dysfunction or bone-related diseases
(such as osteoporosis, rheumatoid arthritis or osteoarthritis); for
improving glycaemic control and/or reducing fasting plasma glucose,
postprandial plasma glucose and/or the glycosylated haemoglobin
HbA1c; for preventing, delaying, slowing or reversing the
progression of disrupted glucose tolerance, insulin resistance
and/or metabolic syndrome to type 2 diabetes; for preventing,
delaying, slowing the progression of or treating a condition or a
disease selected from among the complications of diabetes, such as
for example retinopathy, nephropathy or neuropathies, diabetic
foot, ulcers or macroangiopathies; for reducing weight or
preventing weight gain or assisting weight loss; for preventing or
treating the degradation of pancreatic beta cells and/or improving
and/or restoring the functionality of pancreatic beta cells and/or
restoring the functionality of pancreatic insulin secretion; for
maintaining and/or improving insulin sensitivity and/or preventing
or treating hyperinsulinaemia and/or insulin resistance.
In particular, the compounds and pharmaceutical compositions
according to the invention are suitable for the treatment of
obesity, diabetes (comprising type 1 and type 2 diabetes,
preferably type 2 diabetes mellitus) and/or complications of
diabetes (such as for example retinopathy, nephropathy or
neuropathies, diabetic foot, ulcers or macroangiopathies).
The compounds according to the invention are most particularly
suitable for treating type 2 diabetes mellitus.
The dose range of the compounds of general formula I applicable per
day is usually from 0.001 to 20 mg per kg body weight, for example
from 0.01 to 8 mg per kg body weight of the patient. Each dosage
unit may conveniently contain from 0.1 to 1000 mg, for example 0.5
to 500 mg.
The actual therapeutically effective amount or therapeutic dosage
will of course depend on factors known by those skilled in the art
such as age and weight of the patient, route of administration and
severity of disease. In any case the compound or composition will
be administered at dosages and in a manner which allows a
therapeutically effective amount to be delivered based upon
patient's unique condition.
The compounds, compositions, including any combinations with one or
more additional therapeutic agents, according to the invention may
be administered by oral, transdermal, inhalative, parenteral or
sublingual route. Of the possible methods of administration, oral
or intravenous administration is preferred.
Pharmaceutical Compositions
Suitable preparations for administering the compounds of formula I,
optionally in combination with one or more further therapeutic
agents, will be apparent to those with ordinary skill in the art
and include for example tablets, pills, capsules, suppositories,
lozenges, troches, solutions, syrups, elixirs, sachets,
injectables, inhalatives and powders etc. Oral formulations,
particularly solid forms such as e.g. tablets or capsules are
preferred. The content of the pharmaceutically active compound(s)
is advantageously in the range from 0.1 to 90 wt.-%, for example
from to 70 wt.-% of the composition as a whole.
Suitable tablets may be obtained, for example, by mixing one or
more compounds according to formula I with known excipients, for
example inert diluents, carriers, disintegrants, adjuvants,
surfactants, binders and/or lubricants. The tablets may also
consist of several layers. The particular excipients, carriers
and/or diluents that are suitable for the desired preparations will
be familiar to the skilled man on the basis of his specialist
knowledge. The preferred ones are those that are suitable for the
particular formulation and method of administration that are
desired. The preparations or formulations according to the
invention may be prepared using methods known per se that are
familiar to the skilled man, such as for example by mixing or
combining at least one compound of formula I according to the
invention, or a pharmaceutically acceptable salt of such a
compound, and one or more excipients, carriers and/or diluents.
Combination Therapy
The compounds of the invention may further be combined with one or
more, preferably one additional therapeutic agent. According to one
embodiment the additional therapeutic agent is selected from the
group of therapeutic agents useful in the treatment of diseases or
conditions described hereinbefore, in particular associated with
metabolic diseases or conditions such as for example diabetes
mellitus, obesity, diabetic complications, hypertension,
hyperlipidemia. Additional therapeutic agents which are suitable
for such combinations include in particular those which for example
potentiate the therapeutic effect of one or more active substances
with respect to one of the indications mentioned and/or which allow
the dosage of one or more active substances to be reduced.
Therefore a compound of the invention may be combined with one or
more additional therapeutic agents selected from the group
consisting of antidiabetic agents, agents for the treatment of
overweight and/or obesity and agents for the treatment of high
blood pressure, heart failure and/or atherosclerosis.
Antidiabetic agents are for example metformin, sulphonylureas,
nateglinide, repaglinide, thiazolidinediones, PPAR-(alpha, gamma or
alpha/gamma) agonists or modulators, alpha-glucosidase inhibitors,
DPPIV inhibitors, SGLT2-inhibitors, insulin and insulin analogues,
GLP-1 and GLP-1 analogues or amylin and amylin analogues, cycloset,
11.beta.-HSD inhibitors. Other suitable combination partners are
inhibitors of protein tyrosinephosphatase 1, substances that affect
deregulated glucose production in the liver, such as e.g.
inhibitors of glucose-6-phosphatase, or
fructose-1,6-bisphosphatase, glycogen phosphorylase, glucagon
receptor antagonists and inhibitors of phosphoenol pyruvate
carboxykinase, glycogen synthase kinase or pyruvate dehydrokinase,
alpha2-antagonists, CCR-2 antagonists or glucokinase activators.
One or more lipid lowering agents are also suitable as combination
partners, such as for example HMG-CoA-reductase inhibitors,
fibrates, nicotinic acid and the derivatives thereof, PPAR-(alpha,
gamma or alpha/gamma) agonists or modulators, PCSK9 inhibitors,
PPAR-delta agonists, ACAT inhibitors or cholesterol absorption
inhibitors such as, bile acid-binding substances such as,
inhibitors of ileac bile acid transport, MTP inhibitors, or
HDL-raising compounds such as CETP inhibitors or ABC1
regulators.
Therapeutic agents for the treatment of overweight and/or obesity
are for example antagonists of the cannabinoid1 receptor, MCH-1
receptor antagonists, MC4 receptor agonists, NPY5 or NPY2
antagonists, .beta.3-agonists, leptin or leptin mimetics, agonists
of the 5HT2c receptor.
Therapeutic agents for the treatment of high blood pressure,
chronic heart failure and/or atherosclerosis are for example A-II
antagonists or ACE inhibitors, ECE inhibitors, diuretics,
.beta.-blockers, Ca-antagonists, centrally acting
antihypertensives, antagonists of the alpha-2-adrenergic receptor,
inhibitors of neutral endopeptidase, thrombocyte aggregation
inhibitors and others or combinations thereof are suitable.
Angiotensin II receptor antagonists are preferably used for the
treatment or prevention of high blood pressure and complications of
diabetes, often combined with a diuretic such as
hydrochlorothiazide.
The dosage for the combination partners mentioned above is usually
1/5 of the lowest dose normally recommended up to 1/1 of the
normally recommended dose.
Preferably, compounds of the present invention and/or
pharmaceutical compositions comprising a compound of the present
invention optionally in combination with one or more additional
therapeutic agents are administered in conjunction with exercise
and/or a diet.
Therefore, in another aspect, this invention relates to the use of
a compound according to the invention in combination with one or
more additional therapeutic agents described hereinbefore and
hereinafter for the treatment of diseases or conditions which may
be affected or which are mediated by the activation of the
AMP-activated protein kinase (AMPK), in particular diseases or
conditions as described hereinbefore and hereinafter.
In yet another aspect the present invention relates a method for
treating a disease or condition mediated by the activation of the
AMP-activated protein kinase (AMPK) in a patient that includes the
step of administering to the patient, preferably a human, in need
of such treatment a therapeutically effective amount of a compound
of the present invention in combination with a therapeutically
effective amount of one or more additional therapeutic agents
described in hereinbefore and hereinafter,
The use of the compound according to the invention in combination
with the additional therapeutic agent may take place simultaneously
or at staggered times.
The compound according to the invention and the one or more
additional therapeutic agents may both be present together in one
formulation, for example a tablet or capsule, or separately in two
identical or different formulations, for example as a so-called
kit-of-parts.
Consequently, in another aspect, this invention relates to a
pharmaceutical composition which comprises a compound according to
the invention and one or more additional therapeutic agents
described hereinbefore and hereinafter, optionally together with
one or more inert carriers and/or diluents.
Other features and advantages of the present invention will become
apparent from the following more detailed Examples which
illustrate, by way of example, the principles of the invention.
EXAMPLES
Preliminary Remarks:
As a rule, .sup.1H-NMR and/or mass spectra have been obtained for
the compounds prepared. The R.sub.f values are determined using
Merck silica gel 60 F.sub.254 plates and UV light at 254 nm.
The terms "ambient temperature" and "room temperature" are used
interchangeably and designate a temperature of about 20.degree.
C.
Analytical HPLC parameters employed for characterization of
products (TFA denotes trifluoroacetic acid and FA denotes formic
acid):
TABLE-US-00002 Method: 1 Device: Agilent 1200 with DA and MS
detector Column: XBridge C18, 3.0 .times. 30 mm, 2.5 .mu.m Column
Supplier: Waters Gradient/ % Solvent Solvent [H.sub.2O, % Solvent
Flow Temperature Time [min] 0.1% TFA] [Acetonitrile] [mL/min]
[.degree. C.] 0.00 97 3 2.2 60 0.20 97 3 2.2 60 1.20 0 100 2.2 60
1.25 0 100 3 60 1.40 0 100 3 60
TABLE-US-00003 Method: 2 Device: Agilent 1200 with DA and MS
detector Column: Sunfire C18, 3.0 .times. 30 mm, 2.5 .mu.m Column
Supplier: Waters Gradient/ Solvent % Solvent % Solvent Flow
Temperature Time [min] [H.sub.2O, 0.1% TFA] [CH.sub.3CN] [mL/min]
[.degree. C.] 0.00 97 3 2.2 60 0.20 97 3 2.2 60 1.20 0 100 2.2 60
1.25 0 100 3 60 1.40 0 100 3 60
TABLE-US-00004 Method: 3 Device: Agilent 1200 with DA and MS
detector Column: Sunfire C18, 3.0 .times. 30 mm, 2.5 .mu.m Column
Supplier: Waters Gradient/ % Solvent Solvent [H.sub.2O, % Solvent
Flow Temperature Time [min] 0.1% TFA] [Acetonitrile] [mL/min]
[.degree. C.] 0.00 50 50 2.2 60 0.20 50 50 2.2 60 1.20 0 100 2.2 60
1.25 0 100 3 60 1.40 0 100 3 60
TABLE-US-00005 Method: 4 Device: Agilent 1100 with DA and MS
detector Column: Sunfire C18, 4.6 .times. 30 mm, 3.5 .mu.m Column
Supplier: Waters Gradient/ % Solvent Solvent [H.sub.2O, % Solvent
Flow Temperature Time [min] 0.1% TFA] [Acetonitrile] [mL/min]
[.degree. C.] 0.00 95 5 4.0 60 0.15 95 5 4.0 60 1.70 0 100 4.0 60
2.25 0 100 4.0 60
TABLE-US-00006 Method: 5 Device: Agilent 1200 with DA and MS
detector Column: XBridge C18, 3 .times. 30 mm, 2.5 .mu.m Column
Supplier: Waters Gradient/ Solvent % Solvent % Solvent Flow
Temperature Time [min] [H.sub.2O, 0.1% TFA] [CH.sub.3CN] [mL/min]
[.degree. C.] 0.00 97 3 2.2 60 0.20 97 3 2.2 60 1.20 0 100 2.2 60
1.25 0 100 3 60 1.40 0 100 3 60
The Examples that follow are intended to illustrate the present
invention without restricting it:
Intermediate 1
(3R,3aR,6R,6aR)-6-(6-Chloro-5-iodo-3-(2-trimethylsilanyl-ethoxymethyl)-3H--
imidazo[4,5-b]pyridin-2-yloxy)hexahydrofuro[3,2-b]furan-3-ol
##STR00019##
Step 1:
6-Chloro-5-iodo-2-(methylsulfonyl)-3-(2-trimethylsilanyl-ethoxymet-
hyl)-3H-imidazo[4,5-b]pyridine
6-Chloro-5-iodo-2-(methylsulfonyl)-1H-imidazo[4,5-b]pyridine (for
preparation see WO 2012116145; 1.5 g) and triethylamine (875 .mu.L)
are dissolved in tetrahydrofurane (12 mL), cooled to 0.degree. C.
and treated with (2-(chloromethoxy)ethyl)trimethylsilane (SEM-Cl;
890 .mu.L). The mixture is stirred for 30 minutes while warming to
room temperature. Then the mixture is partitioned between saturated
aqueous NH.sub.4Cl and ethylacetate. The organic phase is washed
with water and brine. After drying (MgSO.sub.4) the solvents are
evaporated in vacuo to give the title compound. LC (method 1):
t.sub.R=1.22 min; Mass spectrum (ESI.sup.+): m/z=488
[M+H].sup.+.
Step 2:
(3R,3aR,6R,6aR)-6-(6-Chloro-5-iodo-3-(2-trimethylsilanyl-ethoxymet-
hyl)-3H-imidazo[4,5-b]pyridin-2-yloxy)hexahydrofuro[3,2-b]furan-3-ol
(3R,3aR,6R,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diol (1.84 g) is
dissolved in N,N-dimethylformamide (10 mL) and treated with
1,8-diazabicyclo[5.4.0]undec-7-ene (DBU; 1.9 mL). A solution of
6-chloro-5-iodo-2-(methylsulfonyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-
-imidazo[4,5-b]pyridine (2.05 g) in N,N-dimethylformamide (20 mL)
is added drop wise and the mixture is stirred for 2 hours at room
temperature. The mixture is partitioned between water and
ethylacetate and the organic phase is washed with brine and dried
(MgSO.sub.4). The solvents are evaporated in vacuo and the residue
is chromatographed on silica gel (cyclohexane/ethyl acetate
80:20.fwdarw.0:100) to give the title compound. LC (method 1):
t.sub.R=1.17 min; Mass spectrum (ESI.sup.+): m/z=554
[M+H].sup.+.
Intermediate 2
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5-y-
l)phenyl]-2-fluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
##STR00020##
Step 1:
(3R,3aR,6R,6aR)-6-(6-Chloro-5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxab-
orolan-2-yl)phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazo[4,5-b]p-
yridin-2-yloxy)hexahydrofuro[3,2-b]furan-3-ol
A mixture of
(3R,3aR,6R,6aR)-6-(6-chloro-5-iodo-3-(2-trimethylsilanyl-ethoxymethyl)-3H-
-imidazo[4,5-b]pyridin-2-yloxy)hexahydrofuro[3,2-b]furan-3-ol (2.00
g), 1,4-benzenediboronic acid dipinacol ester (2.38 g), saturated
aqueous solution of Na.sub.2CO.sub.3 (5.42 mL), and 1,4-dioxane
(15.00 mL) is purged with argon for 5 min.
[1,1'-Bis-(diphenylphosphino)-ferrrocen]-dichlorpalladium(II)-CH.sub.2Cl.-
sub.2-complex (206 mg) is added and the mixture is stirred
overnight at 70.degree. C. The reaction mixture is washed with
water and brine, dried over MgSO.sub.4, and concentrated in vacuo.
The residue is chromatographed on silica gel
(dichloromethane/methanol 99:1.fwdarw.97:3) to give the title
compound. LC (method 1): t.sub.R=1.28 min; Mass spectrum
(ESI.sup.+): m/z=630 [M+H].sup.+.
Step 2:
[(4-Bromo-2-fluorophenyl)imino]dimethyl-.lamda..sup.6-sulfanone
S,S-Dimethylsulfoximine (186 mg) and Cs.sub.2CO.sub.3 (758 mg) are
added to a solution of 4-bromo-2-fluoro-1-iodo-benzene (500 mg) in
1,4-dioxane (15 mL) and the mixture is purged with argon for
several minutes. 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene
(Xantphos, 72 mg) and tris(dibenzylideneacetone)dipalladium(0) (46
mg) are added and the reaction mixture is stirred for 3 h at
100.degree. C. After cooling to room temperature methanol is added
and the mixture is filtered through Celite. The filtrate is
concentrated in vacuo and the residue is chromatographed on silica
gel (cyclohexane/ethyl acetate 70:30.fwdarw.50:50).
LC (method 2): t.sub.R=0.98 min; Mass spectrum (ESI.sup.+): m/z=266
[M+H].sup.+.
Step 3:
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3--
yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyr-
idin-5-yl)phenyl]-2-fluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
A saturated aqueous solution of Na.sub.2CO.sub.3 (875 .mu.L) is
added to a mixture of
(3R,3aR,6R,6aR)-6-(6-chloro-5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan--
2-yl)phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazo[4,5-b]pyridin--
2-yloxy)hexahydrofuro[3,2-b]furan-3-ol (440 mg) and
[(4-bromo-2-fluorophenyl)imino]dimethyl-.lamda..sup.6-sulfanone
(230 mg) in 1,4-dioxane (8 mL) and the resulting mixture is purged
with argon for 5 min.
Bis-(diphenylphosphino)-ferrrocen]-dichlorpalladium(II)-CH.sub.2Cl-
.sub.2-complex (58 mg) is added and the reaction mixture is stirred
overnight at 80.degree. C. After cooling to room temperature the
mixture is diluted with water and dichloromethane.
The organic phase is separated, dried over MgSO.sub.4 and
concentrated in vacuo. The residue is dissolved in a mixture of
tetrahydrofuran/methanol/N,N-dimethylformamide (2:1:1) and
filtered. The filtrate is directly submitted to HPLC on reversed
phase to give the title compound. LC (method 2): t.sub.R=1.13 min;
Mass spectrum (ESI.sup.+): m/z=689 [M+H].sup.+
Intermediate 3
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5-y-
l)phenyl]-3,5-difluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
##STR00021##
Step 1:
[(4-Bromo-3,5-difluorophenyl)imino]dimethyl-.lamda..sup.6-sulfanon-
e
The title compound is prepared from
2-bromo-1,3-difluoro-5-iodo-benzene and S,S-dimethylsulfoximine
following a procedure analogous to that described for Intermediate
2 (Step 2). LC (method 2): t.sub.R=0.95 min; Mass spectrum
(ESI.sup.+): m/z=284 [M+H].sup.+.
Step 2:
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3--
yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyr-
idin-5-yl)phenyl]-3,5-difluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanon-
e
The title compound is prepared from
(3R,3aR,6R,6aR)-6-(6-chloro-5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan--
2-yl)phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazo[4,5-b]pyridin--
2-yloxy)hexahydrofuro[3,2-b]furan-3-ol and
[(4-bromo-3,5-difluorophenyl)imino]dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Intermediate
2 (Step 3). LC (method 2): t.sub.R=1.15 min; Mass spectrum
(ESI.sup.+): m/z=707 [M+H].sup.+.
Intermediate 4
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5-y-
l)phenyl]-2,5-difluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
##STR00022##
Step 1:
[(4-Bromo-2,5-difluorophenyl)imino]dimethyl-.lamda..sup.6-sulfanon-
e
The title compound is prepared from
1-bromo-2,5-difluoro-4-iodo-benzene and S,S-dimethylsulfoximine
following a procedure analogous to that described for Intermediate
2 (Step 2). LC (method 2): t.sub.R=0.93 min; Mass spectrum
(ESI.sup.+): m/z=284 [M+H].sup.+.
Step 2:
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3--
yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyr-
idin-5-yl)phenyl]-2,5-difluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanon-
e
The title compound is prepared from
(3R,3aR,6R,6aR)-6-(6-chloro-5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan--
2-yl)phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazo[4,5-b]pyridin--
2-yloxy)hexahydrofuro[3,2-b]furan-3-ol and
[(4-bromo-2,5-difluorophenyl)imino]dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Intermediate
2 (Step 3). LC (method 2): t.sub.R=1.15 min; Mass spectrum
(ESI.sup.+): m/z=707 [M+H].sup.+.
Intermediate 5
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5-y-
l)phenyl]-2,6-difluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
##STR00023##
Step 1:
[(4-Bromo-2,6-difluorophenyl)imino]dimethyl-.lamda..sup.6-sulfanon-
e
The title compound is prepared from
5-bromo-1,3-difluoro-2-iodobenzene and S,S-dimethylsulfoximine
following a procedure analogous to that described for Intermediate
2 (Step 2). LC (method 2): t.sub.R=0.90 min; Mass spectrum
(ESI.sup.+): m/z=284 [M+H].sup.+.
Step 2:
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3--
yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyr-
idin-5-yl)phenyl]-2,6-difluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanon-
e
The title compound is prepared from
(3R,3aR,6R,6aR)-6-(6-chloro-5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan--
2-yl)phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazo[4,5-b]pyridin--
2-yloxy)hexahydrofuro[3,2-b]furan-3-ol and
[(4-bromo-2,6-difluorophenyl)imino]dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Intermediate
2 (Step 3). LC (method 2): t.sub.R=1.14 min; Mass spectrum
(ESI.sup.+): m/z=707 [M+H].sup.+.
Intermediate 6
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5-y-
l)phenyl]-3-fluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
##STR00024##
Step 1:
[(4-Bromo-3-fluorophenyl)imino]dimethyl-.lamda..sup.6-sulfanone
The title compound is prepared from 1-bromo-2-fluoro-4-iodo-benzene
and S,S-dimethylsulfoximine following a procedure analogous to that
described for Intermediate 2 (Step 2). LC (method 2): t.sub.R=0.91
min; Mass spectrum (ESI.sup.+): m/z=284 [M+H].sup.+.
Step 2:
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3--
yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyr-
idin-5-yl)phenyl]-3-fluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
The title compound is prepared from
(3R,3aR,6R,6aR)-6-(6-chloro-5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan--
2-yl)phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazo[4,5-b]pyridin--
2-yloxy)hexahydrofuro[3,2-b]furan-3-ol and
[(4-bromo-3-fluorophenyl)imino]dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Intermediate
2 (Step 3). LC (method 2): t.sub.R=1.13 min; Mass spectrum
(ESI.sup.+): m/z=689 [M+H].sup.+.
Intermediate 7
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5-y-
l)phenyl]-2,3-difluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
##STR00025##
Step 1:
[(4-Bromo-2,3-difluorophenyl)imino]dimethyl-.lamda..sup.6-sulfanon-
e
The title compound is prepared from
1-bromo-2,3-difluoro-4-iodo-benzene and S,S-dimethylsulfoximine
following a procedure analogous to that described for Intermediate
2 (Step 2). LC (method 2): t.sub.R=0.93 min; Mass spectrum
(ESI.sup.+): m/z=284 [M+H].sup.+.
Step 2:
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3--
yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyr-
idin-5-yl)phenyl]-2,3-difluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanon-
e
The title compound is prepared from
(3R,3aR,6R,6aR)-6-(6-chloro-5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan--
2-yl)phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazo[4,5-b]pyridin--
2-yloxy)hexahydrofuro[3,2-b]furan-3-ol and
[(4-bromo-2,3-difluorophenyl)imino]dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Intermediate
2 (Step 3). LC (method 2): t.sub.R=1.15 min; Mass spectrum
(ESI.sup.+): m/z=707 [M+H].sup.+.
Intermediate 8
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidazo[4,5-b]pyridin-5-yl)-3-
-fluorophenyl]phenyl}-imino)dimethyl-.lamda..sup.6-sulfanone
##STR00026##
Step 1:
(3R,3aR,6R,6aR)-6-{[5-(4-Bromo-2-fluorophenyl)-6-chloro-3-{[2-(tri-
methylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-2-yl]oxy}-hexahydrofur-
o[3,2-b]furan-3-ol
A mixture of
(3R,3aR,6R,6aR)-6-(6-chloro-5-iodo-3-(2-trimethylsilanyl-ethoxymethyl)-3H-
-imidazo[4,5-b]pyridin-2-yloxy)hexahydrofuro[3,2-b]furan-3-ol (500
mg), (4-bromo-2-fluorophenyl)boronic acid (220 mg), and aqueous
Na.sub.2CO.sub.3 solution (2 M, 2.71 mL) in 1,4-dioxane is purged
with argon for 5 min.
[1,1'-Bis-(diphenylphosphino)-ferrrocen]-dichlorpalladium(II)-CH.sub.2Cl.-
sub.2-complex (37 mg) is added and the mixture is stirred at
90.degree. C. for 4 h. The reaction mixture is diluted with ethyl
actate, washed with water and brine, dried over MgSO.sub.4, and
concentrated in vacuo. The residue is chromatographed on silica gel
(cyclohexane/ethyl acetate 50:50.fwdarw.0:100) to give the title
compound. LC (method 3): t.sub.R=0.94 min; Mass spectrum
(ESI.sup.+): m/z=600 [M+H].sup.+.
Step 2:
Dimethyl({[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]imino})-.-
lamda..sup.6-sulfanone
A mixture of [(4-bromophenyl)imino]dimethyl-.lamda..sup.6-sulfanone
(1.58 g), bis(pinacolato)diboron (2.00 g), and K.sub.2CO.sub.3
(2.20 g) in 1,4-dioxane is purged with argon for 10 min.
[1,1'-Bis-(diphenylphosphino)-ferrrocen]-dichlorpalladium(II)-CH.sub.2Cl.-
sub.2-complex (520 mg) is added and the mixture is stirred
overnight at 90.degree. C. After cooling to room temperature the
reaction mixture is filtrated, concentrated in vacuo, and submitted
to silica gel chromatography (dichloromethane/methanol
99:1.fwdarw.97:3) to give the title compound. LC (method 2):
t.sub.R=0.96 min; Mass spectrum (ESI.sup.+): m/z=296
[M+H].sup.+.
Step 3:
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3--
yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidazo[4,5-b]pyridin-
-5-yl)-3-fluorophenyl]phenyl}imino)dimethyl-.lamda..sup.6-sulfanone
The title compound is prepared from
(3R,3aR,6R,6aR)-6-{[5-(4-bromo-2-fluorophenyl)-6-chloro-3-{[2-(trimethyls-
ilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-2-yl]oxy}-hexahydrofuro[3,2-b-
]furan-3-ol and
dimethyl({[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]imino})-.lamda..-
sup.6-sulfanone following a procedure analogous to that described
under Step 2. LC (method 2): t.sub.R=1.11 min; Mass spectrum
(ESI.sup.+): m/z=689 [M+H].sup.+.
Intermediate 9
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidazo[4,5-b]pyridin-5-yl)-2-
-fluorophenyl]phenyl}-imino)dimethyl-.lamda..sup.6-sulfanone
##STR00027##
Step 1:
(3R,3aR,6R,6aR)-6-{[5-(4-Bromo-3-fluorophenyl)-6-chloro-3-{[2-(tri-
methyl-silyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-2-yl]oxy}-hexahydrofu-
ro[3,2-b]furan-3-ol
The title compound is prepared from
(3R,3aR,6R,6aR)-6-(6-chloro-5-iodo-3-(2-trimethylsilanyl-ethoxymethyl)-3H-
-imidazo[4,5-b]pyridin-2-yloxy)hexahydrofuro[3,2-b]furan-3-ol and
(4-bromo-3-fluorophenyl)boronic acid following a procedure
analogous to that described for Intermediate 8 (Step 1). LC (method
3): t.sub.R=0.99 min; Mass spectrum (ESI.sup.+): m/z=600
[M+H].sup.+.
Step 2:
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3--
yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidazo[4,5-b]pyridin-
-5-yl)-2-fluorophenyl]phenyl}imino)dimethyl-.lamda..sup.6-sulfanone
The title compound is prepared from
(3R,3aR,6R,6aR)-6-{[5-(4-bromo-3-fluorophenyl)-6-chloro-3-{[2-(trimethyls-
ilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-2-yl]oxy}-hexahydrofuro[3,2-b-
]furan-3-ol and
dimethyl({[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]imino})-.lamda..-
sup.6-sulfanone following a procedure analogous to that described
for Intermediate 8 (Step 3). LC (method 2): t.sub.R=1.18 min; Mass
spectrum (ESI.sup.+): m/z=689 [M+H].sup.+.
Intermediate 10
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidazo[4,5-b]pyridin-5-yl)-2-
,3-difluorophenyl]-phenyl}imino)dimethyl-.lamda..sup.6-sulfanone
##STR00028##
Step 1:
(3R,3aR,6R,6aR)-6-{[5-(4-Bromo-2,3-difluorophenyl)-6-chloro-3-{[2--
(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-2-yl]oxy}-hexahydr-
ofuro[3,2-b]furan-3-ol
The title compound is prepared from
(3R,3aR,6R,6aR)-6-(6-chloro-5-iodo-3-(2-trimethylsilanyl-ethoxymethyl)-3H-
-imidazo[4,5-b]pyridin-2-yloxy)hexahydrofuro[3,2-b]furan-3-ol and
(4-bromo-2,3-difluorophenyl)boronic acid following a procedure
analogous to that described for Intermediate 8 (Step 1). LC (method
3): t.sub.R=0.96 min; Mass spectrum (ESI.sup.+): m/z=618
[M+H].sup.+.
Step 2:
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3--
yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidazo[4,5-b]pyridin-
-5-yl)-2,3-difluorophenyl]phenyl}imino)dimethyl-.lamda..sup.6-sulfanone
The title compound is prepared from
(3R,3aR,6R,6aR)-6-{[5-(4-bromo-2,3-difluorophenyl)-6-chloro-3-{[2-(trimet-
hylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-2-yl]oxy}-hexahydrofuro[3-
,2-b]furan-3-ol and
dimethyl({[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]imino})-.lamda..-
sup.6-sulfanone following a procedure analogous to that described
for Intermediate 8 (Step 3). LC (method 2): t.sub.R=1.13 min; Mass
spectrum (ESI.sup.+): m/z=707 [M+H].sup.+.
Intermediate 11
({6-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5-y-
l)phenyl]-5-fluoropyridin-3-yl}imino)dimethyl-.lamda..sup.6-sulfanone
##STR00029##
Step 1:
((3R,3aR,6R,6aR)-6-({5-[4-(5-Bromo-3-fluoropyridin-2-yl)phenyl]-6--
chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-2-yl}-
oxy)-hexahydrofuro-[3,2-b]furan-3-ol
The title compound is prepared from
(3R,3aR,6R,6aR)-6-(6-chloro-5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan--
2-yl)phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazo[4,5-b]pyridin--
2-yloxy)hexahydrofuro[3,2-b]furan-3-ol and
5-bromo-3-fluoro-2-iodo-pyridine following a procedure analogous to
that described for Intermediate 2 (Step 3). LC (method 2):
t.sub.R=1.32 min; Mass spectrum (ESI.sup.+): m/z=677
[M+H].sup.+.
Step 2:
({6-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3--
yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyr-
idin-5-yl)phenyl]-5-fluoropyridin-3-yl}imino)dimethyl-.lamda..sup.6-sulfan-
one
The title compound is prepared from
((3R,3aR,6R,6aR)-6-({5-[4-(5-bromo-3-fluoropyridin-2-yl)phenyl]-6-chloro--
3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-2-yl}oxy)-he-
xahydrofuro[3,2-b]furan-3-ol and S,S-dimethylsulfoximine following
a procedure analogous to that described for Intermediate 2 (Step
2). LC (method 2): t.sub.R=1.09 min; Mass spectrum (ESI.sup.+):
m/z=690 [M+H].sup.+.
Intermediate 12
({4-[5-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5-y-
l)-6-methoxypyridin-2-yl]phenyl}imino)dimethyl-.lamda..sup.6-sulfanone
##STR00030##
Step 1:
(3R,3aR,6R,6aR)-6-{[6-Chloro-5-(6-chloro-2-methoxypyridin-3-yl)-3--
{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-2-yl]oxy}-hexa-
hydrofuro[3,2-b]furan-3-ol
The title compound is prepared from
(3R,3aR,6R,6aR)-6-(6-chloro-5-iodo-3-(2-trimethylsilanyl-ethoxymethyl)-3H-
-imidazo[4,5-b]pyridin-2-yloxy)hexahydrofuro[3,2-b]furan-3-ol and
(6-chloro-2-methoxypyridin-3-yl)boronic acid following a procedure
analogous to that described for Intermediate 8 (Step 1). LC (method
2): t.sub.R=1.25 min; Mass spectrum (ESI.sup.+): m/z=569
[M+H].sup.+.
Step 2:
({4-[5-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3--
yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyr-
idin-5-yl)-6-methoxypyridin-2-yl]phenyl}imino)dimethyl-.lamda..sup.6-sulfa-
none
The title compound is prepared from
(3R,3aR,6R,6aR)-6-{[6-chloro-5-(6-chloro-2-methoxypyridin-3-yl)-3-{[2-(tr-
imethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-2-yl]oxy}-hexahydrofu-
ro[3,2-b]furan-3-ol and
dimethyl({[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]imino})-.lamda..-
sup.6-sulfanone following a procedure analogous to that described
for Intermediate 8 (Step 3). LC (method 2): t.sub.R=1.10 min; Mass
spectrum (ESI.sup.+): m/z=702 [M+H].sup.+.
Intermediate 13
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-fluoro-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-imidazo[4,5-b]pyridin-5-y-
l)phenyl]phenyl}-imino)dimethyl-.lamda..sup.6-sulfanone
##STR00031##
Step 1:
{[4-(4-Bromophenyl)phenyl]imino}dimethyl-.lamda..sup.6-sulfanone
The title compound is prepared from 4-bromo-4'-iodobiphenyl and
S,S-dimethylsulfoximine following a procedure analogous to that
described for Intermediate 2 (Step 2). LC (method 5): t.sub.R=0.98
min; Mass spectrum (ESI.sup.+): m/z=284 [M+H].sup.+.
Step 2:
Dimethyl({4-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]phenyl}-
imino)-.lamda..sup.6-sulfanone
The title compound is prepared from
{[4-(4-bromophenyl)phenyl]imino}dimethyl-.lamda..sup.6-sulfanone
and bis(pinacolato)diboron following a procedure analogous to that
described for Intermediate 8 (Step 2). LC (method 5): t.sub.R=1.01
min; Mass spectrum (ESI.sup.+): m/z=372 [M+H].sup.+.
Step 3:
(3R,3aR,6R,6aR)-6-[(5-Bromo-6-fluoro-1-{[2-(trimethylsilyl)ethoxy]-
methyl}-1H-imidazo[4,5-b]pyridin-2-yl)oxy]-hexahydrofuro[3,2-b]furan-3-ol
Potassium tert-butoxide (217 mg) is added to an ice-cooled mixture
of isomannide (282 mg) and
5-bromo-2-chloro-6-fluoro-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-imidazo-
[4,5-b]pyridine (WO 2013/011932, p. 82-83; 490 mg) in
tetrahydrofuran (20 mL) under an argon atmosphere. The resulting
mixture is stirred at room temperature for 2 d. Ethyl acetate is
added and the mixture is washed with water and brine, dried over
MgSO.sub.4 and concentrated in vacuo. The residue is
chromatographed on silica gel (dichloromethane/methanol
97:3.fwdarw.80:20) to give the title compound. LC (method 1):
t.sub.R=1.07 min; Mass spectrum (ESI.sup.+): m/z=490
[M+H].sup.+.
Step 4:
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3--
yl]oxy}-6-fluoro-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-imidazo[4,5-b]pyr-
idin-5-yl)phenyl]phenyl}imino)dimethyl-.lamda..sup.6-sulfanone
A mixture of
(3R,3aR,6R,6aR)-6-[(5-bromo-6-fluoro-1-{[2-(trimethylsilyl)ethoxy]-methyl-
}-1H-imidazo[4,5-b]pyridin-2-yl)oxy]-hexahydrofuro[3,2-b]furan-3-ol
(150 mg),
dimethyl({4-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]phenyl}im-
ino)-.lamda..sup.6-sulfanone (136 mg), and aqueous Na.sub.2CO.sub.3
solution (2 M, 0.61 mL) in N,N-dimethylformamide (6 mL) is purged
with argon for several minutes.
Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)
(13 mg) is added and the mixture is stirred at 70.degree. C. for 3
h. The reaction mixture is allowed to cool to room temperature,
diluted with water, and extracted with ethyl acetate. The combined
extracts are washed with brine, dried over MgSO.sub.4, and
concentrated in vacuo. The crude product is purified by column
chromatography on silica gel (ethyl acetate/methanol
95:5.fwdarw.70:30) to give the title compound. LC (method 1):
t.sub.R=1.07 min; Mass spectrum (ESI.sup.+): m/z=655
[M+H].sup.+.
Intermediate 14
{4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-6-
-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5-yl-
)phenyl]-3-fluorophenyl}(imino)methyl-.lamda..sup.6-sulfanone
##STR00032##
Step 1: 1-Bromo-2-fluoro-4-methanesulfinylbenzene
3-Chloroperoxybenzoic acid id added slowly to an ice-cooled
solution of 4-bromo-3-fluorothioanisole (1.00 g) in and the
resulting mixture is stirred for 1 h. The ice bath is removed and
the mixture is stirred for 2 h at room temperature. The reaction
mixture is diluted with dichloromethane (20 mL), washed with a
saturated aqueous solution of NaHCO.sub.3 and water, dried over
MgSO.sub.4, and concentrated in vacuo. The crude product is used
for the next reaction step without further purification. Mass
spectrum (ESI.sup.+): m/z=237 [M+H].sup.+.
Step 2:
(3R,3aR,6R,6aR)-6-({6-Chloro-5-[4-(2-fluoro-4-methanesulfinylpheny-
l)phenyl]-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-2--
yl}oxy)-hexahydrofuro[3,2-b]furan-3-ol
The title compound is prepared from
(3R,3aR,6R,6aR)-6-(6-chloro-5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan--
2-yl)phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazo[4,5-b]pyridin--
2-yloxy)hexahydrofuro[3,2-b]furan-3-ol and
1-bromo-2-fluoro-4-methanesulfinylbenzene following a procedure
analogous to that described for Intermediate 2 (Step 3). LC (method
2): t.sub.R=1.14 min; Mass spectrum (ESI.sup.+): m/z=284
[M+H].sup.+.
Step 3:
N-({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan--
3-yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]p-
yridin-5-yl)phenyl]-3-fluorophenyl}(methyl)oxo-.lamda..sup.6-sulfanylidene-
)-2,2,2-trifluoroacetamide
A mixture of
(3R,3aR,6R,6aR)-6-({6-chloro-5-[4-(2-fluoro-4-methanesulfinyl-phenyl)phen-
yl]-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-2-yl}oxy-
)-hexahydrofuro[3,2-b]furan-3-ol (200 mg), 2,2,2-trifluoroacetamide
(68 mg), iodobenzene diacetate (146 mg), magnesium oxide (49 mg),
and rhodium(II) acetate dimer (3 mg) in dichloromethane (2 mL) is
stirred overnight at room temperature. The reaction mixture is
diluted with dichloromethane and filtered. The filtrate is washed
with water and brine, dried over MgSO.sub.4, and concentrated in
vacuo. The crude product is used in the next reaction step without
further purification. LC (method 2): t.sub.R=1.23 min; Mass
spectrum (ESI.sup.+): m/z=771 [M+H].sup.+.
Step 4:
{4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-y-
l]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyri-
din-5-yl)phenyl]-3-fluorophenyl}(imino)methyl-.lamda..sup.6-sulfanone
A mixture of
N-({4-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]ox-
y}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin--
5-yl)phenyl]-3-fluorophenyl}(methyl)oxo-.lamda..sup.6-sulfanylidene)-2,2,2-
-trifluoroacetamide (217 mg) and potassium carbonate (130 mg) in
methanol (4 mL) is stirred at room temperature for 2 h. The
reaction mixture is diluted with dichloromethane, washed with
water, dried over MgSO.sub.4, and concentrated in vacuo. The crude
product is used in the next reaction step without further
purification. LC (method 2): t.sub.R=1.06 min; Mass spectrum
(ESI.sup.+): m/z=675 [M+H].sup.+.
Intermediate 15
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-fluoro-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-imidazo[4,5-b]pyridin-5-y-
l)phenyl]-3-fluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
##STR00033##
Step 1:
(3R,3aR,6R,6aR)-6-({6-Fluoro-5-[4-(tetramethyl-1,3,2-dioxaborolan--
2-yl)phenyl]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-imidazo[4,5-b]pyridin-
-2-yl}oxy)-hexahydrofuro[3,2-b]furan-3-ol
The title compound is prepared from
(3R,3aR,6R,6aR)-6-[(5-bromo-6-fluoro-1-{[2-(trimethylsilyl)ethoxy]methyl}-
-1H-imidazo[4,5-b]pyridin-2-yl)oxy]-hexahydrofuro[3,2-b]furan-3-ol
and 1,4-benzenediboronic acid dipinacol ester following a procedure
analogous to that described for Intermediate 2 (Step 1). LC (method
3): t.sub.R=0.92 min; Mass spectrum (ESI.sup.+): m/z=614
[M+H].sup.+.
Step 2:
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3--
yl]oxy}-6-fluoro-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-imidazo[4,5-b]pyr-
idin-5-yl)phenyl]-3-fluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
The title compound is prepared from
(3R,3aR,6R,6aR)-6-({6-fluoro-5-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)ph-
enyl]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-imidazo[4,5-b]pyridin-2-yl}o-
xy)-hexahydrofuro[3,2-b]furan-3-ol and
[(4-bromo-3-fluorophenyl)-imino]dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Intermediate
2 (Step 3). LC (method 2): t.sub.R=1.13 min; Mass spectrum
(ESI.sup.+): m/z=284 [M+H].sup.+.
Intermediate 16
({4-[5-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-imidazo[4,5-b]pyridin-5-yl)-6-methoxypyridin-2-yl]-3-fluorophenyl-
}imino)dimethyl-.lamda..sup.6-sulfanone
##STR00034##
Step 1:
{[3-Fluoro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]imino}dim-
ethyl-A.sup.6 sulfanone
The title compound is prepared from
[(4-bromo-3-fluorophenyl)imino]dimethyl-A.sup.6 sulfanone and
bis(pinacolato)diboron following a procedure analogous to that
described for Intermediate 8 (Step 2). LC (method 2): t.sub.R=0.98
min; Mass spectrum (ESI.sup.+): m/z=314 [M+H].sup.+.
Step 2:
({4-[5-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3--
yl]oxy}-6-chloro-3H-imidazo[4,5-b]pyridin-5-yl)-6-methoxypyridin-2-yl]-3-f-
luorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
The title compound is prepared from
(3R,3aR,6R,6aR)-6-{[6-chloro-5-(6-chloro-2-methoxypyridin-3-yl)-3-{[2-(tr-
imethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-2-yl]oxy}-hexahydrofu-
ro[3,2-b]furan-3-ol and
{[3-fluoro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]imino}dimethyl-.-
lamda..sup.6-sulfanone following a procedure analogous to that
described for Intermediate 8 (Step 3). LC (method 2): t.sub.R=1.13
min; Mass spectrum (ESI.sup.+): m/z=720 [M+H].sup.+.
Intermediate 17
{[4-(4-Bromo-3,5-difluorophenyl)phenyl]imino}dimethyl-.lamda..sup.6-sulfan-
one
##STR00035##
Aqueous Na.sub.2CO.sub.3 solution (2 M, 4.30 mL) is added to
mixture of
dimethyl({[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]imino})-.lamda..-
sup.6-sulfanone (1.00 g) and 4-bromo-3,5-difluoroiodobenzene (1.30
g) in 1,4-dioxane (10 mL) and the resulting mixture is purged with
argon for several minutes.
[1,1'-Bis-(diphenylphosphino)-ferrrocen]-dichlorpalladium(II)-CH.sub.2Cl.-
sub.2-complex (277 mg) is added and the mixture is stirred
overnight at 80.degree. C. The reaction mixture is diluted with 30
mL of water and 30 mL of ethyl acetate and filtered. The aqueous
phase is separated and extracted with 30 mL of ethyl acetate. The
combined organic phases are washed with water and brine, dried over
MgSO.sub.4 and concentrated in vacuo. The crude product is purified
by column chromatography on silica gel (cyclohexane/ethyl acetate
50:50.fwdarw.0:100) to give the title compound. LC (method 2):
t.sub.R=1.09 min; Mass spectrum (ESI.sup.+): m/z=284
[M+H].sup.+.
Intermediate 18
({4-[4-(2-{[(3R,3aR,6R,6aS)-6-[(tert-Butyldimethylsilyl)oxy]-hexahydrofuro-
[3,2-b]furan-3-yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidaz-
o[4,5-b]pyridin-5-yl)-3,5-difluorophenyl]phenyl}imino)dimethyl-.lamda..sup-
.6-sulfanone
##STR00036##
Step 1:
2-{[(3R,3aR,6R,6aS)-6-[(tert-Butyldimethylsilyl)oxy]-hexahydrofuro-
[3,2-b]furan-3-yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidaz-
o[4,5-b]pyridin-5-ylboronic Acid
Isopropylmagensium chloride-lithium chloride complex (1.3 M, 1.27
mL) is added drop wise to a stirred solution of
(3R,3aR,6R,6aR)-6-(6-chloro-5-iodo-3-(2-trimethylsilanyl-ethoxymethyl)-3H-
-imidazo[4,5-b]pyridin-2-yloxy)hexahydrofuro[3,2-b]furan-3-ol (1.00
g) in tetrahydrofuran (10 mL) cooled in an acetone/dry ice bath
under an argon atmosphere. After 30 min a solution of
2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxoborolane (0.35 g) in
tetrahydrofuran (3 mL) is added drop wise and the resulting mixture
is stirred for 1 h. The cooling bath is removed and the reaction
mixture is stirred overnight at room temperature. The reaction is
quenched with aqueous ammonium chloride solution (10%) and
extracted with ethyl acetate. The combined extracts are
concentrated in vacuo and the crude product is used in the next
reaction step without further purification. LC (method 2):
t.sub.R=1.00 min; Mass spectrum (ESI.sup.+): m/z=586
[M+H].sup.+.
Step 2:
({4-[4-(2-{[(3R,3aR,6R,6aS)-6-[(tert-Butyldimethylsilyl)oxy]-hexah-
ydrofuro[3,2-b]furan-3-yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methy-
l}imidazo[4,5-b]pyridin-5-yl)-3,5-difluorophenyl]phenyl}imino)dimethyl-.la-
mda..sup.6-sulfanone
Aqueous potassium phosphate solution (0.5 M; 0.68 mL) is added to a
mixture of
{[4-(4-bromo-3,5-difluorophenyl)phenylhenyl]imino}dimethyl-.lamda..sup.6--
sulfanone (74 mg) and
2-{[(3R,3aR,6R,6aS)-6-[(tert-butyldimethylsilyl)oxy]-hexahydrofuro[3,2-b]-
furan-3-yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidazo[4,5-b-
]pyridin-5-ylboronic acid (100 mg) in 1,4-dioxane (3 mL) in a
microwave vial and the resulting mixture is purged with argon for 1
min.
Chloro(2-dicyclohexylphosphino-2',4',6'-triisopropyl-1,1'-biphenyl)[2-(2'-
-amino-1,1'-biphenyl)]palladium(II) (6.71 mg) is added, the mixture
is again purged with argon, the vial is capped, and the reaction
mixture is stirred for 1 h at room temperature. After standing
overnight ethyl acetate and water are added and the organic phase
is separated, washed with water and brine, dried over MgSO.sub.4,
and concentrated in vacuo. The residue is chromatographed on silica
gel (cyclohexane/ethyl acetate 50:50.fwdarw.20:80) to give the
title compound. LC (method 3): t.sub.R=1.19 min; Mass spectrum
(ESI.sup.+): m/z=821 [M+H].sup.+.
Intermediate 19
({4-[4-(2-{[(3R,3aR,6R,6aS)-6-[(tert-Butyldimethylsilyl)oxy]-hexahydrofuro-
[3,2-b]furan-3-yl]oxy}-6-fluoro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidaz-
o[4,5-b]pyridin-5-yl)-3,5-difluorophenyl]phenyl}imino)dimethyl-.lamda..sup-
.6-sulfanone
##STR00037##
Step 1:
4-(2-{[(3R,3aR,6R,6aS)-6-[(tert-Butyldimethylsilyl)oxy]-hexahydrof-
uro[3,2-b]furan-3-yl]oxy}-6-fluoro-3-{[2-(trimethylsilyl)ethoxy]methyl}imi-
dazo[4,5-b]pyridin-5-yl)-3,5-difluorophenol
The title compound is prepared from
2-{[(3R,3aR,6R,6aS)-6-[(tert-butyldimethylsilyl)oxy]-hexahydrofuro[3,2-b]-
furan-3-yl]oxy}-5-bromo-6-fluoro-3-{[2-(trimethylsilyl)ethoxy]methyl}imida-
zo[4,5-b]pyridine and 2,6-difluoro-4-hydroxy-phenylboronic acid
following a procedure analogous to that described for Intermediate
18 (Step 2). LC (method 3): t.sub.R=1.20 min; Mass spectrum
(ESI.sup.+): m/z=284 [M+H].sup.+. Step 2:
4-(2-{[(3R,3aR,6R,6aS)-6-[(tert-Butyldimethylsilyl)oxy]-hexahydrofuro[3,2-
-b]furan-3-yl]oxy}-6-fluoro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidazo[4,-
5-b]pyridin-5-yl)-3,5-difluorophenyl trifluoromethanesulfonate
Trifluoromethansulfonic anhydride (1 M in dichloromethane; 0.18 mL)
is added to
4-(2-{[(3R,3aR,6R,6aS)-6-[(tert-butyldimethylsilyl)oxy]-hexahydr-
ofuro[3,2-b]furan-3-yl]oxy}-6-fluoro-3-{[2-(trimethylsilyl)ethoxy]methyl}i-
midazo[4,5-b]pyridin-5-yl)-3,5-difluorophenol (100 mg) in
dichloromethane (2 mL) at 0.degree. C. and the resulting mixture is
stirred at this temperature for 1 h. The reaction mixture is
diluted with dichloromethane and aqueous ammonium chloride solution
(10%). The organic phase is separated, washed with aqueous ammonium
chloride solution (10%), dried over MgSO.sub.4, and concentrated in
vacuo. The crude product is used without further purification for
the next reaction step. LC (method 3): t.sub.R=1.32 min; Mass
spectrum (ESI.sup.+): m/z=786 [M+H].sup.+.
Step 3:
({4-[4-(2-{[(3R,3aR,6R,6aS)-6-[(tert-Butyldimethylsilyl)oxy]-hexah-
ydrofuro[3,2-b]furan-3-yl]oxy}-6-fluoro-3-{[2-(trimethylsilyl)ethoxy]methy-
l}imidazo[4,5-b]pyridin-5-yl)-3,5-difluorophenyl]phenyl}imino)dimethyl-.la-
mda..sup.6-sulfanone
The title compound is prepared from
4-(2-{[(3R,3aR,6R,6aS)-6-[(tert-butyldimethylsilyl)oxy]-hexahydrofuro[3,2-
-b]furan-3-yl]oxy}-6-fluoro-3-{[2-(trimethyl-silyl)ethoxy]methyl}imidazo[4-
,5-b]pyridin-5-yl)-3,5-difluorophenyl trifluoromethanesulfonate and
dimethyl({[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]imino})-.lamda..-
sup.6-sulfanone following a procedure analogous to that described
for Intermediate 8 (Step 3). LC (method 3): t.sub.R=1.17 min.
Example 1
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3H-imidazo[4,5-b]pyridin-5-yl)phenyl]-2-fluorophenyl}imino)dimeth-
yl-.lamda..sup.6-sulfanone
##STR00038##
A mixture of
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-
-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5--
yl)phenyl]-2-fluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
(37 mg) and KHSO.sub.4 (2 M aqueous solution, 27 .mu.L) in formic
acid (1 mL) is stirred for 2 h at 65.degree. C. The mixture is
cooled to 0.degree. C. in an ice bath, the pH is adjusted to 11 by
adding NaOH (10 M aqueous solution) and the mixture is stirred for
1.5 h. Hydrochloric acid (4 N) is added until the pH reaches 6. The
mixture is diluted with water and the precipitate is filtered off
and washed with water. The solid residue is rinsed from the filter
with 1,4-dioxane and the solvent is removed by freeze drying to
give the title compound. LC (method 2): t.sub.R=0.89 min; Mass
spectrum (ESI.sup.+): m/z=559 [M+H].sup.+.
Example 2
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3H-imidazo[4,5-b]pyridin-5-yl)phenyl]-3,5-difluorophenyl}imino)di-
methyl-.lamda..sup.6-sulfanone
##STR00039##
The title compound is prepared from
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-
-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5--
yl)phenyl]-3,5-difluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Example 1. LC
(method 2): t.sub.R=0.92 min; Mass spectrum (ESI.sup.+): m/z=577
[M+H].sup.+.
Example 3
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3H-imidazo[4,5-b]pyridin-5-yl)phenyl]-2,5-difluorophenyl}imino)di-
methyl-.lamda..sup.6-sulfanone
##STR00040##
The title compound is prepared from
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-
-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5--
yl)phenyl]-2,5-difluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Example 1. LC
(method 2): t.sub.R=0.91 min; Mass spectrum (ESI.sup.+): m/z=577
[M+H].sup.+.
Example 4
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3H-imidazo[4,5-b]pyridin-5-yl)phenyl]-2,6-difluorophenyl}imino)di-
methyl-.lamda..sup.6-sulfanone
##STR00041##
The title compound is prepared from
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-
-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5--
yl)phenyl]-2,6-difluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Example 1. LC
(method 2): t.sub.R=0.90 min; Mass spectrum (ESI.sup.+): m/z=577
[M+H].sup.+.
Example 5
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3H-imidazo[4,5-b]pyridin-5-yl)phenyl]-3-fluorophenyl}imino)dimeth-
yl-.lamda..sup.6-sulfanone
##STR00042##
The title compound is prepared from
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-
-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5--
yl)phenyl]-3-fluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Example 1. LC
(method 2): t.sub.R=0.89 min; Mass spectrum (ESI.sup.+): m/z=559
[M+H].sup.+.
Example 6
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3H-imidazo[4,5-b]pyridin-5-yl)phenyl]-2,3-difluorophenyl}imino)di-
methyl-.lamda..sup.6-sulfanone
##STR00043##
The title compound is prepared from
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-
-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5--
yl)phenyl]-2,3-difluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Example 1. LC
(method 2): t.sub.R=0.91 min; Mass spectrum (ESI.sup.+): m/z=577
[M+H].sup.+.
Example 7
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3H-imidazo[4,5-b]pyridin-5-yl)-3-fluorophenyl]phenyl}imino)dimeth-
yl-.lamda..sup.6-sulfanone
##STR00044##
The title compound is prepared from
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-
-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidazo[4,5-b]pyridin-5-yl)--
3-fluorophenyl]phenyl}imino)dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Example 1. LC
(method 2): t.sub.R=0.88 min; Mass spectrum (ESI.sup.+): m/z=559
[M+H].sup.+.
Example 8
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3H-imidazo[4,5-b]pyridin-5-yl)-2-fluorophenyl]phenyl}imino)dimeth-
yl-.lamda..sup.6-sulfanone
##STR00045##
The title compound is prepared from
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-
-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidazo[4,5-b]pyridin-5-yl)--
2-fluorophenyl]phenyl}imino)dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Example 1. LC
(method 2): t.sub.R=0.89 min; Mass spectrum (ESI.sup.+): m/z=559
[M+H].sup.+.
Example 9
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3H-imidazo[4,5-b]pyridin-5-yl)-2,3-difluorophenyl]phenyl}imino)di-
methyl-.lamda..sup.6-sulfanone
##STR00046##
The title compound is prepared from
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-
-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidazo[4,5-b]pyridin-5-yl)--
2,3-difluorophenyl]phenyl}imino)dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Example 1. LC
(method 2): t.sub.R=0.90 min; Mass spectrum (ESI.sup.+): m/z=577
[M+H].sup.+.
Example 10
({6-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3H-imidazo[4,5-b]pyridin-5-yl)phenyl]-5-fluoropyridin-3-yl}imino)-
dimethyl-.lamda..sup.6-sulfanone
##STR00047##
The title compound is prepared from
({6-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-
-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5--
yl)phenyl]-5-fluoropyridin-3-yl}imino)dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Example 1. LC
(method 4): t.sub.R=0.94 min; Mass spectrum (ESI.sup.+): m/z=560
[M+H].sup.+.
Example 11
({4-[5-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3H-imidazo[4,5-b]pyridin-5-yl)-6-methoxypyridin-2-yl]phenyl}imino-
)dimethyl-.lamda..sup.6-sulfanone
##STR00048##
The title compound is prepared from
({4-[5-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-
-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5--
yl)-6-methoxypyridin-2-yl]phenyl}imino)dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Example 1. LC
(method 2): t.sub.R=0.87 min; Mass spectrum (ESI.sup.+): m/z=572
[M+H].sup.+.
Example 12
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-fluoro-1H-imidazo[4,5-b]pyridin-5-yl)phenyl]phenyl}imino)dimethyl-.lamda-
..sup.6-sulfanone
##STR00049##
Trifluoroacetic acid (0.57 mL) is added to
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-
-6-fluoro-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-imidazo[4,5-b]pyridin-5--
yl)phenyl]phenyl}imino)dimethyl-.lamda..sup.6-sulfanone (96 mg) in
dichloromethane (5 mL) and the resulting mixture is stirred at room
temperature for 28 h. The reaction mixture is concentrated in vacuo
and the residue is dissolved in ethyl acetate and methanol. The
solution is washed with a saturated aqueous solution of NaHCO.sub.3
and brine, dried over MgSO.sub.4, and concentrated in vacuo. The
residue is triturated with a small amount of methanol, filtered
off, and dried to give the title compound. LC (method 1):
t.sub.R=0.81 min; Mass spectrum (ESI.sup.+): m/z=525
[M+H].sup.+.
Example 13
{4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-6-
-chloro-3H-imidazo[4,5-b]pyridin-5-yl)phenyl]-3-fluorophenyl}(imino)methyl-
-.lamda..sup.6-sulfanone
##STR00050##
The title compound is prepared from
{4-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridin-5-y-
l)phenyl]-3-fluorophenyl}(imino)methyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Example 1. LC
(method 2): t.sub.R=0.83 min; Mass spectrum (ESI.sup.+): m/z=545
[M+H].sup.+.
Example 14
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-fluoro-1H-imidazo[4,5-b]pyridin-5-yl)phenyl]-3-fluorophenyl}imino)dimeth-
yl-.lamda..sup.6-sulfanone
##STR00051##
The title compound is prepared from
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-
-6-fluoro-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-imidazo[4,5-b]pyridin-5--
yl)phenyl]-3-fluorophenyl}imino)dimethyl-.lamda..sup.6-sulfanone
following a procedure analogous to that described for Example 1. LC
(method 2): t.sub.R=0.88 min; Mass spectrum (ESI.sup.+): m/z=543
[M+H].sup.+.
Example 15
({4-[5-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-3H-imidazo[4,5-b]pyridin-5-yl)-6-methoxypyridin-2-yl]-3-fluorophe-
nyl}imino)dimethyl-.lamda..sup.6-sulfanone
##STR00052##
The title compound is prepared from
({4-[5-(2-{[(3R,3aR,6R,6aR)-6-hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-
-6-chloro-3H-imidazo[4,5-b]pyridin-5-yl)-6-methoxypyridin-2-yl]-3-fluoroph-
enyl}imino)dimethyl-.lamda..sup.6-sulfanone following a procedure
analogous to that described for Example 1. LC (method 2):
t.sub.R=0.90 min; Mass spectrum (ESI.sup.+): m/z=590
[M+H].sup.+.
Example 16
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-fluoro-1H-imidazo[4,5-b]pyridin-5-yl)-3,5-difluorophenyl]phenyl}imino)di-
methyl-.lamda..sup.6-sulfanone
##STR00053##
The title compound is prepared from
({4-[4-(2-{[(3R,3aR,6R,6aS)-6-[(tert-butyldimethylsilyl)oxy]-hexahydrofur-
o[3,2-b]furan-3-yl]oxy}-6-fluoro-3-{[2-(trimethyl-silyl)ethoxy]methyl}imid-
azo[4,5-b]pyridin-5-yl)-3,5-difluorophenyl]phenyl}imino)dimethyl-.lamda..s-
up.6-sulfanone following a procedure analogous to that described
for Example 12. LC (method 2): t.sub.R=0.87 min; Mass spectrum
(ESI.sup.+): m/z=561 [M+H].sup.+.
Example 17
({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}--
6-chloro-1H-imidazo[4,5-b]pyridin-5-yl)-3,5-difluorophenyl]phenyl}imino)di-
methyl-.lamda..sup.6-sulfanone
##STR00054##
The title compound is prepared from
({4-[4-(2-{[(3R,3aR,6R,6aS)-6-[(tert-butyldimethylsilyl)oxy]-hexahydrofur-
o[3,2-b]furan-3-yl]oxy}-6-chloro-3-{[2-(trimethyl-silyl)ethoxy]methyl}imid-
azo[4,5-b]pyridin-5-yl)-3,5-difluorophenyl]phenyl}imino)dimethyl-.lamda..s-
up.6-sulfanone following a procedure analogous to that described
for Example 1. LC (method 2): t.sub.R=0.89 min; Mass spectrum
(ESI.sup.+): m/z=577 [M+H].sup.+.
* * * * *